METHOD FOR THE DEHYDROGENATION OF DICHLOROSILANE

Abstract

Dichlorosilane and trichlorosilane are dehydrogenated at elevated temperature in the presence of an ammonium or phosphonium salt as a catalyst, and a halogenated hydrocarbon or hydrogen halide. The method may be used to synthesize organochlorosilane.

Claims

1.-11. (canceled)

12. A method for the dehydrogenation of dichlorosilane in which hydrogen is formed, comprising: reacting dichlorosilane in the presence of an ammonium and/or phosphonium salt at a temperature within a range of 70-300° C., either with (A) at least one halogenated hydrocarbon of the formula (I)
R.sup.1—X  (I), where X is F, Cl, Br or I; and R.sup.1 is a branched or unbranched C.sub.2-C.sub.20 alkyl radical, a branched or unbranched C.sub.2-C.sub.13 heteroalkyl radical, the carbon skeleton of which contains one or more heteroatoms independently selected from N, P, S or O, a branched or unbranched C.sub.1-C.sub.10 fluoroalkyl radical with partial or complete fluorination, a branched or unbranched C.sub.2-C.sub.20 alkenyl radical, excluding C.sub.2H.sub.4-nCl.sub.n radicals where n is 2-4, a branched or unbranched C.sub.2-C.sub.20 alkynyl radical, a C.sub.3-C.sub.14 cycloalkyl radical, a C.sub.2-C.sub.13 heterocycloalkyl radical, the ring skeleton of which contains one or more heteroatoms independently selected from N, P, S or O, a C.sub.6-C.sub.14 aryl radical, a C.sub.5-C.sub.13 heteroaryl radical, the ring skeleton of which contains one or more heteroatoms independently selected from N, P, S or O, and/or (CH.sub.2).sub.n—Ar, where Ar is a C.sub.6-C.sub.14 aryl radical and n is 1-5, where all of the above-mentioned radicals may be unsubstituted or else singly or multiply substituted by halogen, C.sub.1-C.sub.4 alkoxy, vinyl, phenyl or C.sub.1-C.sub.4 alkyl, radicals, (CH.sub.2).sub.nX, where n is 1-10 and X is F, Cl, Br or I, R.sup.2—S—CH.sub.2 radicals, where R.sup.2 is C.sub.1-C.sub.6 alkyl or C.sub.6-C.sub.14 aryl, (CH.sub.2).sub.nSiMe.sub.3-m—Cl.sub.m, where n is 0-5 and m is 0, 1, 2, 3, (CH.sub.2).sub.nNH(C═O)OCH.sub.3, where n is 1-5, (CH.sub.2).sub.nOCH.sub.2 (oxirane), where n is 1-5, (CH.sub.2).sub.nO(C═O)(C(CH.sub.3)═CH.sub.2), where n is 1-5, (CH.sub.2).sub.nNH.sub.2, where n is 1-5, (CH.sub.2).sub.nNH(C═O)NH.sub.2, where n is 1-5, and (CH.sub.2).sub.nNHR, where n=1-5, and R is cyclohexyl or C.sub.2H.sub.4NH.sub.2; or with (B) a hydrogen halide, wherein the molar ratio of dichlorosilane to hydrogen halide or halogenated hydrocarbon is within a range from 1:1 to 1:10.

13. The method of claim 12, wherein the temperature is within the range of 100-300° C.

14. The method of claim 12, wherein the molar ratio of catalyst to dichlorosilane is within the range from 0.01:1 to 0.2:1.

15. The method of claim 12, wherein a hydrogen halide is present, and the hydrogen halide is hydrogen chloride.

16. The method of claim 12, wherein the ammonium and/or phosphonium salt is a quaternary ammonium halide [R.sub.4N]X, a phosphonium halide [R.sub.4P]X, or a tertiary ammonium halide [R.sub.3NH]X, where X is Cl, Br or I.

17. The method of claim 16, wherein the ammonium and/or phosphonium salt is selected from the group consisting of [n-Bu.sub.4N]Cl, [Et.sub.4N]Cl, [Ph.sub.4P]Cl, [n-Bu.sub.4P]Cl, and mixtures thereof.

18. The method of claim 12, wherein R.sup.1 is selected from the group consisting of branched or unbranched C.sub.2-C.sub.20 alkyl radicals, a branched or unbranched C.sub.2-C.sub.13 heteroalkyl radical, the carbon skeleton of which contains one or more heteroatoms independently selected from N, P, S or O; a branched or unbranched C.sub.2-C.sub.20 alkenyl radical, excluding C.sub.2H.sub.4-nCl.sub.n when n is 2-4, a C.sub.3-C.sub.14 cycloalkyl radical, a C.sub.2-C.sub.13 heterocycloalkyl radical, the ring skeleton of which contains one or more heteroatoms independently selected from N, P, S or O, and (CH.sub.2).sub.n—Ar, where Ar is a C.sub.6-C.sub.14 aryl radical and n is 1-3, where all of the above-mentioned radicals may be unsubstituted or else singly or multiply substituted by halogen, C.sub.1-C.sub.4 alkoxy, vinyl, phenyl or C.sub.1-C.sub.4 alkyl, (CH.sub.2).sub.nX, where n is 1-10 and X is F, Cl, Br or I, (CH.sub.2).sub.nSiMe.sub.3-m—Cl.sub.m, where n is 0-5 and m is 0, 1, 2, 3.

19. The method of claim 12, wherein the halogenated hydrocarbon is selected from the group consisting of methyl chloride, ethyl chloride, n-propyl chloride, isopropyl chloride, n-butyl chloride, tert-butyl chloride, isobutyl chloride, sec-butyl chloride, n-pentyl chloride, n-pentyl iodide, n-pentyl bromide, n-pentyl fluoride, n-octyl chloride, 1-chlorohexadecane, 1,2-dichloroethane, 1,1-dichloropropane, 1,2-dichloropropane, 1,3-dichloropropane, monochlorobenzene, benzyl chloride, vinyl chloride, allyl chloride, allyl bromide, 1-chloro-2,4,4-trimethylpentane, hexadecyl chloride, 1-chloro-3,3,3-trifluoropropane, trichloro(chloromethyl)silane, dichloro(chloromethyl)silane, trimethyl(chloromethyl)silane, trimethyl(3-chloropropyl)silane, crotyl chloride, 4-fluorobenzyl chloride, 4-chlorobenzyl chloride, 4-methoxybenzyl chloride, 4-phenylbenzyl chloride, diphenyl-1-dichloromethane, (1-chloroethyl)benzene, cyclopentyl chloride, 1-bromo-3-chloropropane, 1,4-dichlorobutane, 1,4-bis(chloromethyl)benzene, and mixtures thereof.

20. The method of claim 12, wherein dichlorosilane is formed in situ by disproportionation of trichlorosilane.

21. The method of claim 12, wherein the method is operated continuously or batchwise.

Description

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0038] In the method according to the invention, dichlorosilane is reacted with a halogenated hydrocarbon of the formula (I) or with a hydrogen halide in the presence of an ammonium and/or phosphonium salt as catalyst. Both dichlorosilane and trichlorosilane may be used as reactants in the method according to the invention. Dichlorosilane is dehydrogenated directly by this method. Trichlorosilane, on the other hand, initially disproportionates to tetrachlorosilane and dichlorosilane (reaction scheme 1), which then undergoes dehydrogenation.

##STR00001##

[0039] The dehydrogenation of dichlorosilane proceeds according to reaction scheme 2 below:

##STR00002##

[0040] In a first reaction step, the non-isolable intermediate [SiCl.sub.3] is formed from dichlorosilane with elimination of hydrogen (reaction scheme 2). This anion can either react further through formal nucleophilic substitution or it can insert as dichlorosilylene. In the case of reaction with an R-Cl bond, the product is in both cases a compound R-SiCl.sub.3 and in both cases a chloride ion is liberated again, which is then in turn available as a catalyst (reaction scheme 3):

##STR00003##

[0041] The reaction of the intermediate with a compound R—X (X═F, Br or 1) results in the formation, in addition to a chloride ion, of a compound R—SiCl.sub.3-nX.sub.n (n=0, 1, 2 or 3) as a result of halogen exchange at silicon, which means that a total of 4 products are obtained (reaction scheme 4):

##STR00004##

[0042] If the intermediate reacts for example with HCl, trichlorosilane is formed and a chloride ion is liberated (reaction scheme 5):

##STR00005##

[0043] In the method according to the invention, an ammonium and/or phosphonium salt is used as catalyst. The ammonium and/or phosphonium salt may also be used in immobilized form, for example on a silicone resin, on silica, on an inorganic support or on an organic polymer. The ammonium and/or phosphonium salt may also be formed in situ from an amine or phosphine and HCl.

[0044] Quaternary ammonium halides [R.sub.4N]X and phosphonium halides [R.sub.4P]X or tertiary ammonium halides [R.sub.3NH]X are particularly suitable, where the following applies in each case:

[0045] X═Cl, Br or I, with preference given to Cl or Br, and

[0046] R=independently selected from the group consisting of C.sub.1-C.sub.12 alkyl group, C.sub.1-C.sub.6 alkyl-substituted C.sub.6-C.sub.14 aryl group, and phenyl group, with preference given to ethyl, n-butyl, and phenyl.

[0047] Particularly preferred examples of such compounds are [n-Bu.sub.4N]Cl, [Et.sub.4N]Cl, [Ph.sub.4P]Cl, and [n-Bu.sub.4P]Cl.

[0048] The reactant used is either a hydrogen halide or a halogenated hydrocarbon of the formula (I).

[0049] Hydrogen halide is understood as meaning hydrogen fluoride, hydrogen chloride, hydrogen bromide or hydrogen iodide, with preference given to hydrogen chloride.

R.sup.1—X  (1)

[0050] where

[0051] X═F, Cl, Br or I, and

[0052] R.sup.1=branched or unbranched C.sub.2-C.sub.20 alkyl radical, [0053] branched or unbranched C.sub.2-C.sub.13 heteroalkyl radical, the carbon skeleton containing one or more heteroatoms independently selected from N, P, S or O, [0054] branched or unbranched C.sub.1-C.sub.10 fluoroalkyl radical with partial or complete fluorination, [0055] branched or unbranched C.sub.2-C.sub.20 alkenyl radical, excluding C.sub.2H.sub.4-nCl.sub.n when n=2-4, branched or unbranched C.sub.2-C.sub.20 alkynyl radical, [0056] C.sub.3-C.sub.14 cycloalkyl radical, [0057] C.sub.2-C.sub.13 heterocycloalkyl radical, the ring skeleton containing one or more heteroatoms independently selected from N, P, S or O, [0058] C.sub.6-C.sub.14 aryl radical, [0059] C.sub.5-C.sub.13 heteroaryl radical, the ring skeleton containing one or more heteroatoms independently selected from N, P, S or O, [0060] (CH.sub.2).sub.n—Ar, where Ar═C.sub.6-C.sub.14 aryl radical and n=1-5, [0061] where all of the above-mentioned radicals may be unsubstituted or else singly or multiply substituted by halogen, C.sub.1-C.sub.4 alkoxy, vinyl, phenyl or C.sub.1-C.sub.4 alkyl, methyl radical, [0062] (CH.sub.2).sub.nX, where n=1-10 and X═F, Cl, Br or I, [0063] R.sup.2—S—CH.sub.2 radical, where R.sup.2═C.sub.1-C.sub.6 alkyl or C.sub.6-C.sub.14 aryl, [0064] (CH.sub.2).sub.nSiMe.sub.3-m—Cl.sub.m, where n=0-5 and m=0, 1, 2, 3, [0065] (CH.sub.2).sub.nNH(C═O)OCH.sub.3, where n=1-5, [0066] (CH.sub.2).sub.nOCH.sub.2 (oxirane), where n=1-5, [0067] (CH.sub.2).sub.nO(C═O)(C(CH.sub.3)═CH.sub.2), where n=1-5, [0068] (CH.sub.2).sub.nNH.sub.2, where n=1-5, [0069] (CH.sub.2).sub.nNH(C═O)NH.sub.2, where n=1-5, [0070] (CH.sub.2).sub.nNHR, where n=1-5, and R=cyclohexyl or C.sub.2H.sub.4NH.sub.2.

[0071] R.sup.1 in formula (I) is preferably selected from the group consisting of

[0072] branched or unbranched C.sub.2-C.sub.20 alkyl radical,

[0073] branched or unbranched C.sub.2-C.sub.13 heteroalkyl radical, the carbon skeleton containing one or more heteroatoms independently selected from N, P, S or O;

[0074] branched or unbranched C.sub.2-C.sub.20 alkenyl radical, excluding C.sub.2H.sub.4-nCl.sub.n when n=2-4, C.sub.3-C.sub.14 cycloalkyl radical,

[0075] C.sub.2-C.sub.13 heterocycloalkyl radical, the ring skeleton containing one or more heteroatoms independently selected from N, P, S or O,

[0076] (CH.sub.2).sub.n—Ar, where Ar═C.sub.6-C.sub.14 aryl radical and n=1-3,

[0077] where all of the above-mentioned radicals may be unsubstituted or else singly or multiply substituted by halogen, C.sub.1-C.sub.4 alkoxy, vinyl, phenyl or C.sub.1-C.sub.4 alkyl,

[0078] methyl radical,

[0079] (CH.sub.2).sub.nX, where n=1-10 and X═F, Cl, Br or I,

[0080] (CH.sub.2).sub.nSiMe.sub.3-m—Cl.sub.m, where n=0-5 and m=0, 1, 2, 3.

[0081] Examples of such compounds are:

[0082] methyl chloride, ethyl chloride, n-propyl chloride, isopropyl chloride, n-butyl chloride, tert-butyl chloride, isobutyl chloride, sec-butyl chloride, n-pentyl chloride, n-pentyl iodide, n-pentyl bromide, n-pentyl fluoride, n-octyl chloride, 1-chlorohexadecane, 1,2-dichloroethane, 1,1-dichloropropane, 1,2-dichloropropane, 1,3-dichloropropane, monochlorobenzene, benzyl chloride, vinyl chloride, allyl chloride, allyl bromide, 1-chloro-2,4,4-trimethylpentane, hexadecyl chloride, 1-chloro-3,3,3-trifluoropropane, trichloro(chloromethyl)silane, dichloro(chloromethyl)silane, trimethyl(chloromethyl)silane, trimethyl(3-chloropropyl)silane, crotyl chloride, 4-fluorobenzyl chloride, 4-chlorobenzyl chloride, 4-methoxybenzyl chloride, 4-phenylbenzyl chloride, diphenyl-1-dichloromethane, (1-chloroethyl)benzene, cyclopentyl chloride, 1-bromo-3-chloropropane, 1,4-dichlorobutane, 1,4-bis(chloromethyl)benzene.

[0083] The method according to the invention is carried out at a temperature within a range of 70-300° C. The temperature is preferably within a range of 100-300° C., more preferably within a range of 100-180° C., and yet more preferably within a range of 150-180° C. Most preferably. the temperature is within a range of 170-180° C.

[0084] The molar ratio of hydrogen halide or halogenated hydrocarbon to dichlorosilane may be freely chosen by those skilled in the art.

[0085] In the case of hydrogen halide as the reactant, the amount of hydrogen halide added preferably corresponds to the stoichiometric amount of dichlorosilane to be converted. In the case of all other reactants, the stoichiometric amount of dichlorosilane formally used preferably corresponds to at least the amount of R.sup.1—X bonds to be silylated. If not all the R.sup.1—X bonds are to be silylated, the compound R.sup.1—X is preferably used in a suprastoichiometric amount. The molar ratio of dichlorosilane to hydrogen halide or halogenated hydrocarbon is particularly preferably within a range from 1:1 to 1:10 based on the amount of R.sup.1—X bonds.

[0086] The molar ratio of catalyst to dichlorosilane may be freely chosen by those skilled in the art.

[0087] The molar ratio is preferably within a range from 0.01:1 to 0.2:1.

[0088] The method according to the invention for the dehydrogenation of dichlorosilane allows organosilanes to be prepared in an economical manner. The method also enables dichlorosilane to be converted into trichlorosilane. On the one hand, the dichlorosilane formed as a by-product in the chlorosilane process can in principle be converted into the main product trichlorosilane in this way. Alternatively, mixtures of the two substances may be worked up such that the proportion of dichlorosilane in the mixture is lowered or the mixture is completely converted into trichlorosilane.

EXAMPLES

[0089] GC measurements were performed using an Agilent 6890N (WLD detector; columns: HP5 from Agilent: length: 30 m/diameter: 0.32 mm/film thickness: 0.25 μm; RTX-200 from Restek: length: 60 m/diameter: 0.32 mm/film thickness: 1 μm). Retention times were compared with the commercially available substances, all chemicals were used as purchased. MS measurements were carried out using a ThermoStar™ GSD 320 T2 with an iridium cathode.

[0090] Reactions Starting from Trichlorosilane

Example 1: Synthesis of trichloromethylsilane

[0091] An autoclave was filled with HSiCl.sub.3 (50 g; 0.37 mol), [n-Bu.sub.4N]Cl (0.2 g; 0.7 mmol), and MeCl (9.4 g; 0.19 mol). The autoclave was heated to 140° C. for 13 h. After cooling, approx. 10 bar pressure remained in the autoclave. The product mixture consisted of 30% by weight of Cl.sub.3SiMe, 50% by weight of SiCl.sub.4, and 20% by weight of HSiCl.sub.3, in addition to which traces of MeCl and H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 2: Synthesis of n-propyltrichlorosilane

[0092] An autoclave was filled with HSiCl.sub.3 (40 g; 0.30 mol), [n-Bu.sub.4P]Cl (2 g; 6.8 mmol), and MeCH.sub.2CH.sub.2Cl (10 g; 0.13 mol). The autoclave was heated to 175° C. for 13 h. After cooling, approx. 20 bar pressure remained in the autoclave. The product mixture consisted of 48% by weight of Cl.sub.3SiCH.sub.2CH.sub.2Me, 42% by weight of SiCl.sub.4, 8% by weight of HSiCl.sub.3, and 2% by weight of MeCH.sub.2CH.sub.2Cl, in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 3: Synthesis of 1-chloro-3-trichlorosilylpropane and 1,3-bis (trichlorosilyl)propane

[0093] An autoclave was filled with HSiCl.sub.3 (36.6 g; 0.27 mol), [n-Bu.sub.4P]Cl (2 g; 6.8 mmol), and Cl—CH.sub.2CH.sub.2CH.sub.2—Cl (15.4 g; 0.13 mol). The autoclave was heated to 170° C. for 13 h. After cooling, approx. 10 bar pressure remained in the autoclave. The product mixture consisted of 25% by weight of ClSiCH.sub.2CH.sub.2CH.sub.2Cl, 14% by weight of ClSiCH.sub.2CH.sub.2CH.sub.2SiCl, 14% by weight of ClCH.sub.2CH.sub.2CH.sub.2Cl, 45% by weight of SiCl.sub.4, 2% by weight of HSiCl.sub.3, and traces of H.sub.2SiCl.sub.2. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 4: Synthesis of 1-chloro-3-trichlorosilylpropane

[0094] An autoclave was filled with HSiCl.sub.3 (18 g; 0.13 mol), [n-Bu.sub.4P]Cl (2 g; 6.8 mmol), and Cl—CH.sub.2CH.sub.2CH.sub.2—Cl (30.2 g; 0.27 mol). The autoclave was heated to 170° C. for 13 h. After cooling, approx. 5 bar pressure remained in the autoclave. The product mixture consisted of 21% by weight of ClSiCH.sub.2CH.sub.2CH.sub.2Cl, 1% by weight of ClSiCH.sub.2CH.sub.2CH.sub.2SiCl, 59% by weight of ClCH.sub.2CH.sub.2CH.sub.2Cl, 19% by weight of SiCl.sub.4, and traces of H.sub.2SiCl.sub.2. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 5: Synthesis of allyltrichlorosilane

[0095] An autoclave was filled with HSiCl.sub.3 (20 g; 0.15 mol), [n-Bu.sub.4P]Cl (2 g; 6.8 mmol), and allyl chloride (11.2 g; 0.15 mol). The autoclave was heated to 150° C. for 13 h. After cooling, approx. 15 bar pressure remained in the autoclave. The product mixture consisted of 42% by weight of Cl.sub.3SiCH.sub.2CHCH.sub.2, 40% by weight of SiCl.sub.4, 18% by weight of ClCH.sub.2CHCH.sub.2, and traces of H.sub.2SiCl.sub.2. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

[0096] Reactions Starting from Dichlorosilane

Example 6a) Synthesis of n-propyltrichlorosilane

[0097] An autoclave was filled with H.sub.2SiCl.sub.2 (27 g; 0.27 mol), [n-Bu.sub.4P]Cl (2.5 g; 8 mmol), and MeCH.sub.2CH.sub.2Cl (49.5 g; 0.63 mol). The autoclave was heated to 175° C. for 13 h. After cooling, approx. 45 bar pressure remained in the autoclave. The product mixture consisted of 50% by weight of Cl.sub.3SiCH.sub.2CH.sub.2Me, 2% by weight of SiCl.sub.4, 2% by weight of HSiCl.sub.3, and 46% by weight of MeCH.sub.2CH.sub.2Cl, in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 6b) Synthesis of n-pentyltrichlorosilane

[0098] An autoclave was filled with H.sub.2SiCl.sub.2 (15 g; 0.15 mol), [n-Bu.sub.4P]Cl (2.5 g; 8 mmol), and Me(CH.sub.2).sub.4Cl (50.5 g; 0.48 mol). The autoclave was heated to 177° C. for 13 h. After cooling, approx. 13 bar pressure remained in the autoclave. The product mixture consisted of 45% by weight of Cl.sub.3Si(CH.sub.2).sub.4Me and 55% by weight of Me(CH.sub.2).sub.4Cl, in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 6c) Synthesis of n-pentyltrihalosilane Starting from 1-iodopentane

[0099] An autoclave was filled with H.sub.2SiCl.sub.2 (11 g; 0.11 mol), [n-Bu.sub.4P]Cl (2.0 g; 7 mmol), and Me(CH.sub.2).sub.4I (27.5 g; 0.14 mol). The autoclave was heated to 175° C. for 13 h. After cooling, approx. 16 bar pressure remained in the autoclave. The product mixture consisted of 80% by weight of a mixture of Cl.sub.3-nI.sub.nSi(CH.sub.2).sub.4Me (n=0-3) and 20% by weight of Me(CH.sub.2).sub.4I , in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 6d) Synthesis of n-pentyltrihalosilane Starting from 1-bromopentane

[0100] An autoclave was filled with H.sub.2SiCl.sub.2 (26 g; 0.26 mol), [n-Bu.sub.4P]Cl (2.0 g; 7 mmol), and Me(CH.sub.2).sub.4Br (40.0 g; 0.27 mol). The autoclave was heated to 170° C. for 13 h. After cooling, approx. 33 bar pressure remained in the autoclave. The product mixture consisted of 100% by weight of a mixture of Cl.sub.3-nBr.sub.nSi(CH.sub.2).sub.4Me (n=0-3), in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 6e) Synthesis of n-pentyltrihalosilane Starting from 1-fluoropentane

[0101] An autoclave was filled with H.sub.2SiCl.sub.2 (26 g; 0.26 mol), [n-Bu.sub.4P]Cl (2.0 g; 7 mmol), and Me(CH.sub.2).sub.4F (23.5 g; 0.26 mol). The autoclave was heated to 170° C. for 13 h. After cooling, approx. 10 bar pressure remained in the autoclave. The product mixture consisted of 100% by weight of a mixture of Cl.sub.3-nF.sub.nSi(CH.sub.2).sub.4Me (n=0-3), in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry.

Example 7a) Reaction of dichlorosilane with HCl

[0102] An autoclave was filled with H.sub.2SiCl.sub.2 (17 g; 0.17 mol), HCl (6.2 g; 0.17 mol), [n-Bu.sub.4P]Cl (2.0 g; 7 mmol), and HSiCl.sub.3 (20 g; 0.25 mol). The autoclave was heated to 180° C. for 13 h. After cooling, approx. 19 bar pressure remained in the autoclave. The product consisted of 100% by weight of HSiCl.sub.3, in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry, in addition to which traces of HCl were detectable.

Example 7b) Reaction of Dichlorosilane with HCl

[0103] An autoclave was filled with H.sub.2SiCl.sub.2 (17 g; 0.17 mol), HCl (6.2 g; 0.17 mol), Bu.sub.3N (1.0 g; 5 mmol), and HSiCl.sub.3 (20 g; 0.15 mol). The autoclave was heated to 180° C. for 13 h. After cooling, approx. 19 bar pressure remained in the autoclave. The product consisted of 100% by weight of HSiCl.sub.3, in addition to which traces of H.sub.2SiCl.sub.2 were detectable. The gas evolved in the reaction was unambiguously identified as hydrogen by mass spectrometry, in addition to which traces of HCl were detectable.