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filingDate 2005-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8fcee4f70e1c52f2d21e928f7eca9730
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publicationDate 2006-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7119232-B2
titleOfInvention Nucleophilic substitution reactions of difluorormethyl phenyl sulfone with alkyl halides leading to the facile synthesis of terminal 1,1-difluoro-1-alkenes and difluoromethylalkanes
abstract (Benzenesulfonyl)difluoromethyl anion, in situ generated from difluoromethyl phenyl sulfone and a base, was found to easily undergo nucleophilic substitution reactions (S N 2) with primary alkyl halides, elemental halogens, and perfluoroalkyl halides with good selectivity. The formed (benzenesufonyl)difluoromethylalkanes are useful intermediates for the facile preparation of 1,1-difluoro-1-alkenes and difluoromethylalkanes. Thus, difluoromethyl phenyl sulfone acts as both “CF 2 ═” and “CF 2 H − ” synthons
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