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filingDate 1992-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f12f11236a6e542f49588d47053f2143
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f707ec9bbe9f396cc486b1f99383465d
publicationDate 1992-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0518110-A2
titleOfInvention Process for the preparation of pure enatiomers of 4-[4-(4'-tert.butylphenyl)-2-hydroxybutoxy]-benzoic acid and its alkyl ester
abstract The pure enantiomers of 4- [4- (4'-tert-butylphenyl) -2-hydroxybutoxy] benzoic acid and their alkyl esters can be prepared in surprisingly good yield by reacting the pure enantiomeric forms of S (-) - or R ( +) - 4- (4'-tert-Butylphenyl) -1,2-epoxybutane with 4-hydroxybenzoic acid alkyl ester at elevated temperature in DMF and in the presence of 4-hydroxybenzoic acid alkyl ester sodium salt. The raw reaction product is then to be separated off. Either the stereochemically pure LIFIBROL ester is obtained by recrystallization or the precipitated LIFIBROL enantiomer is prepared in pure, crystalline form by mild alkaline saponification and subsequent acidification.
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priorityDate 1991-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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