Patent classifications
C07C303/40
Method for preparing imide salts containing a fluorosulphonyl group
A fluorination process for obtaining fluorinated compounds including at least one fluorosulfonyl group. More particularly, a process for preparing a fluorinated compound of formula (II), including at least one step of reacting a compound of formula (I) with anhydrous hydrofluoric acid in at least one organic solvent, in which R1 is equal to R2 except in the specific case where R1═Cl, then R2═F, and when R1 is equal to R2, R1 and R2 represent an electron-withdrawing group which has a Hammett parameter σp of greater than 0, such as F, CF.sub.3, CHF.sub.2, CH.sub.2F, C.sub.2HF.sub.4, C.sub.2H.sub.2F.sub.3, C.sub.2H.sub.3F.sub.2, C.sub.2F.sub.5, C.sub.3F.sub.7, C.sub.3H.sub.2F.sub.5, C.sub.3H.sub.4F.sub.3, C.sub.3HF.sub.6, C.sub.4F.sub.9, C.sub.4H.sub.2F.sub.7, C.sub.4H.sub.4F.sub.5, C.sub.5F.sub.11, C.sub.3F.sub.5OCF.sub.3, C.sub.2F.sub.4OCF.sub.3, C.sub.2H.sub.2F.sub.2OCF.sub.3, CF.sub.2OCF.sub.3, C.sub.6F.sub.13, C.sub.7F.sub.15, C.sub.8F.sub.17 or C.sub.9F.sub.19, and M represents a hydrogen atom, an alkali metal, an alkaline-earth metal or a quaternary ammonium cation.
Method for preparing imide salts containing a fluorosulphonyl group
A fluorination process for obtaining fluorinated compounds including at least one fluorosulfonyl group. More particularly, a process for preparing a fluorinated compound of formula (II), including at least one step of reacting a compound of formula (I) with anhydrous hydrofluoric acid in at least one organic solvent, in which R1 is equal to R2 except in the specific case where R1═Cl, then R2═F, and when R1 is equal to R2, R1 and R2 represent an electron-withdrawing group which has a Hammett parameter σp of greater than 0, such as F, CF.sub.3, CHF.sub.2, CH.sub.2F, C.sub.2HF.sub.4, C.sub.2H.sub.2F.sub.3, C.sub.2H.sub.3F.sub.2, C.sub.2F.sub.5, C.sub.3F.sub.7, C.sub.3H.sub.2F.sub.5, C.sub.3H.sub.4F.sub.3, C.sub.3HF.sub.6, C.sub.4F.sub.9, C.sub.4H.sub.2F.sub.7, C.sub.4H.sub.4F.sub.5, C.sub.5F.sub.11, C.sub.3F.sub.5OCF.sub.3, C.sub.2F.sub.4OCF.sub.3, C.sub.2H.sub.2F.sub.2OCF.sub.3, CF.sub.2OCF.sub.3, C.sub.6F.sub.13, C.sub.7F.sub.15, C.sub.8F.sub.17 or C.sub.9F.sub.19, and M represents a hydrogen atom, an alkali metal, an alkaline-earth metal or a quaternary ammonium cation.
Method for preparing imide salts containing a fluorosulphonyl group
A fluorination process for obtaining fluorinated compounds including at least one fluorosulfonyl group. More particularly, a process for preparing a fluorinated compound of formula (II), including at least one step of reacting a compound of formula (I) with anhydrous hydrofluoric acid in at least one organic solvent, in which R1 is equal to R2 except in the specific case where R1═Cl, then R2═F, and when R1 is equal to R2, R1 and R2 represent an electron-withdrawing group which has a Hammett parameter σp of greater than 0, such as F, CF.sub.3, CHF.sub.2, CH.sub.2F, C.sub.2HF.sub.4, C.sub.2H.sub.2F.sub.3, C.sub.2H.sub.3F.sub.2, C.sub.2F.sub.5, C.sub.3F.sub.7, C.sub.3H.sub.2F.sub.5, C.sub.3H.sub.4F.sub.3, C.sub.3HF.sub.6, C.sub.4F.sub.9, C.sub.4H.sub.2F.sub.7, C.sub.4H.sub.4F.sub.5, C.sub.5F.sub.11, C.sub.3F.sub.5OCF.sub.3, C.sub.2F.sub.4OCF.sub.3, C.sub.2H.sub.2F.sub.2OCF.sub.3, CF.sub.2OCF.sub.3, C.sub.6F.sub.13, C.sub.7F.sub.15, C.sub.8F.sub.17 or C.sub.9F.sub.19, and M represents a hydrogen atom, an alkali metal, an alkaline-earth metal or a quaternary ammonium cation.
Process for preparing 4[[(benzoyl)amino]sulphonyl]benzoyl chlorides and preparation of acylsulphamoylbenzamides
Process for preparing 4-[[(benzoyl)amino]sulphonyl]benzoyl chlorides of the formula (II). ##STR00001##
Process for preparing 4[[(benzoyl)amino]sulphonyl]benzoyl chlorides and preparation of acylsulphamoylbenzamides
Process for preparing 4-[[(benzoyl)amino]sulphonyl]benzoyl chlorides of the formula (II). ##STR00001##
Process for preparing 4[[(benzoyl)amino]sulphonyl]benzoyl chlorides and preparation of acylsulphamoylbenzamides
Process for preparing 4-[[(benzoyl)amino]sulphonyl]benzoyl chlorides of the formula (II). ##STR00001##
FLUORINATED AMINE OXIDE SURFACTANTS
Compositions including one or more fluorochemical surfactants of the formula: (I) where R.sub.f is a perfluoroalkyl group, each of R.sup.1, R.sup.2 and R.sup.3 are C.sub.1-C.sub.20 alkyl, alkoxy, or aryl; and R.sup.4 is alkylene, arylene of a combination thereof. R.sup.4 is preferably an alkylene of 1-20 carbons that may be cyclic or acyclic, may optionally contain catenated or terminal heteroatoms selected from the group consisting of N, O, and S. Most preferably R.sup.4 is an alkylene of 2-10 carbon atoms. Described are anionic N-substituted fluorinated amine oxide surfactants, and use thereof in cleaning and in acid etch solutions. The cleaning and etch solutions are used with a wide variety of substrates, for example, in the cleaning and etching of silicon oxide-containing substrates.
##STR00001##
FLUORINATED AMINE OXIDE SURFACTANTS
Compositions including one or more fluorochemical surfactants of the formula: (I) where R.sub.f is a perfluoroalkyl group, each of R.sup.1, R.sup.2 and R.sup.3 are C.sub.1-C.sub.20 alkyl, alkoxy, or aryl; and R.sup.4 is alkylene, arylene of a combination thereof. R.sup.4 is preferably an alkylene of 1-20 carbons that may be cyclic or acyclic, may optionally contain catenated or terminal heteroatoms selected from the group consisting of N, O, and S. Most preferably R.sup.4 is an alkylene of 2-10 carbon atoms. Described are anionic N-substituted fluorinated amine oxide surfactants, and use thereof in cleaning and in acid etch solutions. The cleaning and etch solutions are used with a wide variety of substrates, for example, in the cleaning and etching of silicon oxide-containing substrates.
##STR00001##
Direct oxidative amination of hydrocarbons
Provided is a process for converting a hydrocarbon comprising at least one C—H bond to a nitrogen-functionalized product. The process comprises contacting a hydrocarbon and (i) an oxidizing electrophile comprising (a) a main group element or transition metal in oxidized form and (b) at least one nitrogen-containing ligand, or (ii) an oxidant and a reduced form of an oxidizing electrophile comprising (a) a main group element or transition metal and (b) at least one nitrogen-containing ligand, in a solvent to provide the nitrogen-functionalized product and an electrophile reduction product. Further provided is an oxidizing composition comprising the oxidizing electrophile with at least one nitrogen-containing ligand and a non-oxidizable liquid.
Direct oxidative amination of hydrocarbons
Provided is a process for converting a hydrocarbon comprising at least one C—H bond to a nitrogen-functionalized product. The process comprises contacting a hydrocarbon and (i) an oxidizing electrophile comprising (a) a main group element or transition metal in oxidized form and (b) at least one nitrogen-containing ligand, or (ii) an oxidant and a reduced form of an oxidizing electrophile comprising (a) a main group element or transition metal and (b) at least one nitrogen-containing ligand, in a solvent to provide the nitrogen-functionalized product and an electrophile reduction product. Further provided is an oxidizing composition comprising the oxidizing electrophile with at least one nitrogen-containing ligand and a non-oxidizable liquid.