CONTINUOUS METHOD FOR REACTIONS WITH FINE-PARTICULATE ALKALI METAL DISPERSIONS

Abstract

The invention relates to a method for carrying out organic reactions with fine-particulate alkali metal dispersions in a continuous operation, preferably on a rotary disc reactor. This method can be used primarily in the production of coupling products following Wurtz synthesis, and in the production of macrocycles using acyloin condensation.

Claims

1. A process for performing continuous chemical reactions for the conversion of dispersions of finely divided alkali metals in inert solvents comprising: providing a first metering container containing a liquid alkali metal or alkali metal mixture or alloy, a second metering container containing a reactant or a reactant mixture, a or alloy, a second metering container containing a reactant or a reactant mixture, a third metering container containing a solvent or a solvent mixture, and a spinning disc reactor; introduction of the solvent to the spinning disc reactor; metering the liquid alkali metal or alkali metal mixture or alloy into the spinning disc reactor; and metering the reactant or a reactant mixture into the spinning disc reactor and allowing a chemical process to occur.

2. (canceled)

3. The process according to claim 1, wherein the alkali metal or alkali metal mixture or alloy is lithium, sodium, potassium, mixtures thereof and/or alloys thereof.

4. The process according to claim 1, characterized in that the chemical process is a Wurtz synthesis.

5. The process according to claim 4, characterized in that mono-, di- or multifunctional halogen compounds of the elements of Main Group IV are employed as the reactants for said Wurtz synthesis.

6. The process according to claim 4 for preparing linear, branched and cyclic hydrocarbons from mono-, di- or multifunctional organic halogen compounds and mixtures thereof in the Wurtz synthesis.

7. The process according to claim 5 for preparing polysilanes from mono-, di- or multifunctional halosilanes and mixtures thereof.

8. The process according to claim 8, characterized in that the chemical process is an acyloin condensation.

9. The process according to claim 8, characterized in that organic mono-, di-, tri- or polyester compounds are employed as the reactants for said acyloin condensation.

10. The process according to claim 1, characterized in that said spinning disc reactor has a dwelling time unit connected downstream thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] The present invention is illustrated and described herein with reference to the drawing, in which like reference numbers denote like method steps and/or system components, respectively, and in which:

[0016] FIG. 1 illustrates an exemplary flow diagram of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0017] The reference symbol 1 represents a metering container with liquid alkali metal or alkali metal mixture/alloy; the reference symbol 2 represents a metering container of the reactant or reactant mixture; the reference symbol 3 represents a metering container of the solvent or solvent mixture; the reference symbol 4 represents a spinning disc reactor (SDR); the reference symbol 5 represents an optional dwelling time unit (for example, a stirred tank, a stirred tank cascade, a heat exchanger); the reference symbol 6 represents a collection container of the product mixture; the reference symbol 7 represents a collection container of the by-product mixture.

[0018] Because of the above examples, the spinning disc reactor could be developed as a suitable technology according to the invention for carrying out reactions with liquid alkali metal dispersions in inert organic solvents, especially the Wurtz coupling of halogen compounds, and the acyloin condensation, to form solid precipitates. This type of reactor has been developed for process intensification in order to optimize, in particular, heat transfer (heating, cooling, heat exchange) and mass transport processes (mixing, dispersing): This technology is based on one or more discs which are mounted horizontally on a rotating axis driven by an electric motor. A liquid applied to the surface of this disc is thrown to the edge of the plate or beyond by the action of the centrifugal acceleration. In the formed thin film, high shear forces are acting, and thus there are excellent heat and mass transfer rates. Thus, in highly exothermic reactions, the resulting heat can be dissipated quickly, and the mass transport maximized in diffusion-controlled processes. In addition, the high shear forces introduced in the liquid film flowing through lead to strong turbulence, which offers significant advantages, mainly in reactions in multiphase systems: Because of the high shear forces, the dispersed phase is very finely divided, and the interface between two immiscible phases maximized. This optimizes the mass transport to and from the interface. Further, the rotational motion is strong enough to propel solid deposits from the disc surface, creating a kind of self-cleaning mechanism, the fouling or blocking being reduced by the formation of precipitate.

[0019] The use described in this invention typically takes place in a liquid medium, which consists of an inert solvent or solvent mixture and the reactants dissolved therein (for example, haloalkanes, halosilanes, esters). In general, to achieve a high reaction rate, it is necessary that the alkali metal used or the alkali metal mixture or alloy used be in a molten state to disperse it in a finely divided state in the reaction medium. The alkali metal or alkali metal mixture or alloy, the reactants and solvents are each separately metered into the reactor. In the reaction of the alkali metal or alkali metal mixture or alloy with the reactants, an alkali metal salt insoluble in the reaction mixture is formed, and a coupling product, which may be soluble or insoluble in the liquid medium, depending on the type of reaction. It is thus a continuously performed multiphase reaction in which the reactive phases are present in a liquid form, and one or more reaction products are deposited as a solid precipitate.

[0020] All reaction steps are typically carried out under an inert gas atmosphere, in order to prevent side reactions due to oxygen or humidity, in particular the formation of hydrogen and hydrogen chloride.

[0021] In principle, all alkali metals, their mixtures and/or alloys are suitable for preparing the alkali metal dispersion. Preferred are the alkali metals or mixtures and/or alloys thereof whose melting point is in the range between 20 and 190 C. Especially preferred are lithium, sodium and potassium as well as their mixtures and alloys, since they are technically accessible and melt in a temperature range which is technically easy to handle.

[0022] As suitable inert solvents, all industrially common aprotic organic solvents can be employed in which the reactants (for example, halogen compounds of elements of Main Group IV or organic esters) are soluble, and which do not react with the alkali metal employed, or with the alkali metal mixture or alloy employed. Preferably used are hydrocarbons such as benzene, toluene, xylene and aliphatic hydrocarbons, and ethers such as dioxane, anisole and THF. The inert solvent may also be a mixture of the solvents mentioned, for example, of a hydrocarbon and an ether, i.e., for example, toluene and THF. Typically, the alkali metal salt formed in the reaction is not soluble in the solvent employed and can be separated off by filtration of the precipitate.

[0023] Different substances may be used as said reactants:

[0024] With the inventive method, all substrates common for Wurtz coupling, such as mono-, di-, tri- and polyfunctional alkyl and aryl halides, and mixtures thereof, and mono-, di-, tri- and polyfunctional haloorganosilanes and mixtures thereof can be reacted. Fluorine, chlorine, bromine and iodine can be used as said halogens in the halogen compounds, in particular, chlorine, bromine and iodine, preferably chlorine and bromine, are employed. In particular, the invention is suitable for the preparation of polysilanes and polycarbosilanes of halogenated organosilane building blocks that are no polysilanes. The halogenated organosilane components are defined by comprising less than 5 silicon atoms, preferably up to 3 silicon atoms, more preferably not more than 2 silicon atoms, and most preferably only one silicon atom.

[0025] For acyloin condensation, monoesters, diesters, triesters and polyesters are used. Preferably, mono- and diesters are used. In particular, the method described is suitable for the intramolecular cyclization of dicarboxylic acid esters to medium and large ring systems.

[0026] In the present invention, the amount of the solvent, the alkali metal and the reactants should be selected so that the reaction medium remains fluid even after formation of the solid precipitating alkali metal halides and the insoluble products, if any, so that fouling and blockage of the SDR remain minimized. Typically, from 5 to 99% by weight of solvent is employed, based on the total reaction mixture, preferably from 50 to 97% by weight, more preferably from 70 to 95% by weight of solvent fraction.

[0027] According to the invention, the ratio of the alkali metals employed or their mixtures and/or alloys to the reactants is selected so that a complete conversion is achieved. In the production of low molecular weight coupling products, a stoichiometric use, if possible, is preferred. For the preparation of polymeric coupling products, an excess of the alkali metal with respect to the halide, preferably an excess of up to 20% by weight, more preferably an excess of up to 10% by weight, even more preferably ex excess of up to 5% by weight, is typically required.

[0028] The process described in this invention can be carried out in a wide temperature range. The temperature range is limited by the fact that it is a multistage process with two fluids, more specifically the molten alkali metal or the molten alkali metal mixture or alloy, and the reaction medium of solvent and reactants. Thus, the melting temperature of the alkali metal or the alkali metal alloy/mixture results as the lower limit of the temperature range. The upper limit is determined by the boiling of the reaction mixture and the technical design of SDRs. Preferably, the reaction is carried out in a range between 50 and 200 C., more preferably between 100 and 115 C.

[0029] The rotational speed of the turntable of the SDR must be chosen so that an optimal dispersion of the liquid alkali metal or alkali metal mixture/alloy in the solvent is obtained.

[0030] A further advantage of the present invention is the high ratio of surface to volume of the reaction mixture, and the efficient mixing of this, whereby an efficient removal of the heat quantity generated in the exothermic reaction is possible. This results in a short dwelling time of the reaction mixture in the SDR and hence a short overall process time, with simultaneous reduction of the danger potential of the reaction. The resulting high space-time yield makes the process described economically highly interesting in comparison to established semibatch processes. Typically, the dwelling time of the reaction mixture in the SDR is<10 min, more preferably<5 min. During this time, most of the exothermic heat of the reaction is released and dissipated. In order to maximize the conversion of the reactive groups, especially in the preparation of a polymeric reaction product, a dwelling time unit may optionally be connected downstream. Here, all suitable units known in the art are suitable, in particular, a continuous stirred tank, a stirred tank cascade, a heat exchanger and temperature-controllable loop reactors.

[0031] When the reaction has reached the desired degree of conversion, the reaction product can be separated from the reaction mixture and optionally purified by any suitable method known in the art. For example, if the product is soluble in the reaction medium, the solid alkali metal salt precipitate is first separated off by filtration together with residual alkali metal, if any. Then, the product is obtained, for example, by fractional distillation or by distilling off the solvent. If the product is insoluble in the reaction medium, it can be removed by filtration together with the solid alkali metal salt precipitate and possibly residual alkali metal. Unreacted alkali metal is deactivated, if necessary, with protic solvents, and the alkali metal salts and extracted with water. These are examples.

EXAMPLES

[0032] For the reactions carried out, a commercially available SpinPro Reactor of the Company Flowid (Eindhoven, Netherlands, http://www.flowid.nl/spinpro-reactor/) with three turntables and an integrated heat exchanger was used. The distance between the turntables and the wall was 2 mm. The reactor volume was 230 ml. For all reactions, the reactor was evacuated 20 times for inerting and ventilated with 8 bar nitrogen. For the synthesis of polysilanes (Examples 1 and 2), a continuous stirred tank with a dwelling time of 20 min (flow rate 7.2 kg/h=>2.8 L; flow rate 10.8 kg/h=>4.1 L) was connected downstream of the SDR as a dwelling time unit.

Comparative Example

Semibatch Process for the Preparation of poly(methylphenylsilane)

[0033] Using standard Schlenk techniques, an apparatus comprising a 1000 mL four-necked flask with a dropping funnel, reflux condenser, KPG stirrer and temperature probe was evacuated and flooded with argon. In the four-necked flask, 215 g of xylene and 17.9 g of sodium were charged. The dropping funnel was filled with 67.3 g of dichloromethylphenylsilane, also under an inert gas atmosphere. With slow stirring, the flask was heated in an oil bath to about 102 C., so that the sodium was molten. Now, the agitation speed was set at exactly 300 rpm, and stirring was performed for about five minutes. After this time, a homogeneous, finely divided dispersion was formed (visual evaluation). To this suspension, the dichlorophenylmethylsilane was metered over a period of about 30 minutes. The start of the reaction could be observed by a rise in temperature, as well as an intense violet coloration of the reaction mixture. The metering rate was to be selected such that the dichlorophenylmethylsilane was added uniformly over the metering time while the reaction temperature is always kept within a temperature range of from 102 to 106 C.

[0034] After the end of the metering, the reaction mixture was stirred for a further 2 h at 102 C. After cooling to room temperature, the resulting suspension was filtered through a ceramic frit (G4) under a protective gas. The filtrate was concentrated by distilling off the solvent mixture under vacuum to obtain the soluble fraction of the poly(methylphenylsilane) formed. The polymer was characterized by .sup.1H NMR, .sup.13C NMR, .sup.29Si NMR spectroscopy (each in C.sub.6D.sub.6) and gel permeation chromatography (in THF with light scattering detector).

[0035] Yield: 32%

[0036] Molar mass: 2000 g/mol

[0037] .sup.1H NMR ( [ppm], CDCl.sub.3): 6.5-7.5 ppm, 0.5 ppm

[0038] .sup.13C NMR ( [ppm], CDCl.sub.3): 134-138 ppm, 125-130 ppm, 21 ppm

[0039] .sup.25Si-NMR ( [ppm], CDCl.sub.3): 41 ppm, 40 ppm, 39 ppm, +15 ppm

Example 1Continuous Preparation of poly(methylphenylsilane)

[0040] To start up the reaction, the SDR was adjusted to a rotational speed of 1000 or 2500 rpm, a heating oil temperature of 100 or 105 C., and at first a xylene flow rate of 6.5 kg/h. Once a constant temperature had become established in the reactor, the sodium metering was started. As soon as the discharge of a gray dispersion into the collecting vessel was observed, the metering of the dichloromethylphenylsilane was started. The mass ratio of dichloromethylphenylsilane to sodium was constant at 5/1 in all experiments. The start of the reaction was immediately recognizable by the temperature rise on the first and second plates of the reactor. Later, the deeply violet colored reaction mixture was discharged into the collection container. The metering rates and oil temperatures were varied as listed in the Table.

[0041] The product was filtered under nitrogen through a G4 ceramic frit, and the solvent was distilled off completely under vacuum. The polymer was characterized by .sup.1H NMR, .sup.13C NMR, .sup.2Si NMR spectroscopy (each in C.sub.6D.sub.6) and gel permeation chromatography (in THF with light scattering detector).

TABLE-US-00001 Yield of Revolutions per T.sub.heating oil Total flow Solids T.sub.1st/2nd/3rd plates Molar mass polysilane minute [rpm] [C.] rate [kg/h] content [%] [ C.] [g/mol] [%] 1.1 2500 105 7.2 10 109/107/104 3100 46 1.2 10.8 112/108/105 2900 43 1.3 2500 105 10.8 20 119/114/109 1900 35 1.4 7.2 116/113/108 2200 38 1.5 1000 105 7.2 20 106/111/107 2400 41 1.6 10.8 107/118/109 2100 37 1.7 2500 100 10.8 20 110/106/101 2900 42 1.8 7.2 107/103/100 3200 47

[0042] .sup.1H NMR ( [ppm], CDCl.sub.3): 6.5-7.5 ppm, 0.5 ppm.

[0043] .sup.13C NMR ( [ppm], CDCl.sub.3): 134-138 ppm, 125-130 ppm, 21 ppm.

[0044] .sup.29Si-NMR ( [ppm], CDCl.sub.3): 41 ppm, 40 ppm, 39 ppm, +15 ppm.

Example 2Preparation of Cyclic oligo(methylphenylsilane)

[0045] At a rotation speed of 2500 rpm, a heating oil temperature of 125 C. and a xylene flow rate of 6.5 kg/h, the sodium metering was started at 2 g/min. The temperature in the reactor leveled off at 122 C. As soon as the discharge of a gray dispersion from the reactor was observed, the monomer metering was started at 10 g/min. The start of the reaction was immediately recognizable by the temperature rise in the reactor to 129 C. on the first plate. A little later, the deeply violet colored reaction mixture was discharged into the collection container. The product was filtered under nitrogen, and the solvent was distilled off. The polymer was characterized by .sup.1H NMR, .sup.13C NMR, .sup.29Si NMR spectroscopy (each in C.sub.6D.sub.6) and gel permeation chromatography (in THF with light scattering detector).

[0046] GPC (eluent toluene, RI detector, calibration: polysiloxane standard): 300 g/mol, 900 g/mol

[0047] GPC (eluent THF, LS detector, sample-specific calibration): 1300 g/mol, D=1.6

[0048] .sup.1H NMR ( [ppm], CDCl.sub.3): 6.5-7.5 ppm, 0.5 ppm.

[0049] .sup.13C NMR ( [ppm], CDCl.sub.3): 134-138 ppm, 125-130 ppm, 21 ppm.

[0050] .sup.29Si-NMR ( [ppm], CDCl.sub.3): 41 ppm, 40 ppm, 39 ppm.

[0051] At a rotation speed of 2500 rpm, an oil temperature of 110 C. and a xylene flow rate of 6.5 kg/h, the sodium metering was started at 1.0 g/min. The temperature in the reactor leveled off at 122 C. As soon as the discharge of a gray dispersion from the reactor was observed, the metering of 1.6-dibromohexane was started at. 4 g/min. The start of the reaction was immediately recognizable by the temperature rise in the reactor to 127 C. on the first plate. A little later, the deeply violet colored reaction mixture was discharged into the collection container. The product was filtered off under nitrogen, the composition of the filtrate was analyzed by GC-MS, and a conversion of 98.5% was determined. The pure product was obtained by fractional distillation of the filtrate in 91% yield and analyzed by .sup.1H and .sup.13C NMR spectroscopy.

[0052] .sup.1H NMR ( [ppm], CDCl.sub.3): 1.44.

[0053] .sup.13C NMR ( [ppm], CDCl.sub.3): 26.9.