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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-04
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filingDate 1968-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1970-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1189561-A
titleOfInvention Process for Preparing Fluorinated Organic Sulfonyl Derivatives and Sulfones
abstract 1,189,561. Fluorinated sulphones, sulphonyl fluorides and sulphonic acids. E.I. DU PONT DE NEMOURS & CO. 19 Feb., 1968 [21 Feb., 1967], No. 7914/68. Heading C2C. Polyfluorinated sulphonyl fluorides and polyfluorinated sulphones are prepared by reacting an olefin of the formula or with SO 2 F 2 or a compound of the formula R(SO 2 F) p in the presence of fluoride ion in a polar organic aprotic solvent at 25-200‹C.; in the above formulµ A is fluorine or a perfluorohydrocarbon group which is unsubstituted or is substituted by a single substituent chosen from H, CH 3 and OCH 3 or by up to two halogen substituents other than fluorine provided that the number of such halogen atoms does not exceed the number of fluorine atoms, B is chlorine, fluorine or an unsubstituted or substituted perfluorohydrocarbon group as defined above, or A and B together form a perfluoroalkylene group, the total number of carbon atoms in A and B is from 0 to 8, n is 0 or an integer from 1 to 4, m is an integer from 1 to 6, R is an aliphatic mono- or di-radical containing 1-18 carbon atoms which is free from aliphatic unsaturation and is composed entirely of carbon and one or more of H, halogen, O and S, the O and S being present as ether, sulphone or sulphide, and p is 1 or 2. The invention also comprises perfluorosulphones of the formulµ and wherein A<SP>1</SP> and B<SP>1</SP> are fluorine or perfluoroalkyl, R<SP>1</SP>t is C 1-18 perfluoralkyl, the total number of carbon atoms in each pair of groups A<SP>1</SP> and B<SP>1</SP> attached to the same carbon atom is 0-8, and t is an integer from 2-10. The sulphonyl fluorides may be hydrolysed with a base to form the corresponding sulphonic acid salt which may be subsequently converted to the free acid by treatment with a strong acid.
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priorityDate 1967-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 43.