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filingDate 1991-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6836bbe1356780b142d6406a925e9156
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publicationDate 1992-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04267890-A
titleOfInvention Production of (r)-2-propoxybenzene derivative
abstract PURPOSE: To obtain the subject compound useful as a synthetic intermediate for a pyridobenzoxazine derivative known as a synthetic antibacterial agent in high purity under mild condition by carrying out the asymmetric acylation of a hydroxypropoxybenzene derivative in the presence of an esterase. n CONSTITUTION: An (R)-2-acyloxypropoxybenzene derivative of formula II [-C(0)R 1 is organic acyl] is produced by reacting a (I)-2-hydroxypropoxybenzene derivative of formula I (X 1 and X 2 are halogen), e.g. (±)-2,3-difluoro-6-nitro[(2- hydroxypropyl)oxy]-benzene with an acylation agent consisting of an organic carboxylic acid (preferably acetic anhydride, etc.) in the presence of an esterase. The hydrolysis of the compound of formula II gives an (R)-2- hydroxypropoxybenzene derivative of formula III. The acylation of the compound of formula I is preferably carried out in an ether solvent at 20-50°C. n COPYRIGHT: (C)1992,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02079485-A1
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