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filingDate 1987-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1816b5bf8cf6f1e4ea0ceed9697ced6
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publicationDate 1988-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63227564-A
titleOfInvention Production of allylsulfone
abstract PURPOSE: To obtain the titled compound useful as a drug intermediate in high yield, by reacting a readily obtainable tertiary allyl halide with a phenylsulfinate in the presence of a halogenated tetraalkylammonium salt in an anhydrous system. n CONSTITUTION: A tertiary allyl halide shown by formula I (X is Cl, Br or I) and/or a primary allyl halide shown by formula II is reacted with a phenylsulfinate shown by formula III (R is H or lower alkyl; m is Na or K) in the presence of a halogenated tetraalkylammonium salt in an anhydrous system to give an allylsulfone shown by formula IV (double bond does not distinguish stereospecificity). The compound shown by formula IV is useful as a synthetic intermediate for vitamin A acetate. n COPYRIGHT: (C)1988,JPO&Japio
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Total number of triples: 31.