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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-377
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filingDate 2003-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc4c3847bbc193d68a52b32d2da92a62
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publicationDate 2004-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004217608-A
titleOfInvention Method for producing (1S, 2S) -2-fluorocyclopropanecarboxylic acid derivative
abstract [Object] To provide a simple and selective method for producing an optically active compound useful as an intermediate for producing an antibacterial drug. [Construction] It is manufactured according to the following manufacturing process. Embedded image (Wherein, R 1 and R 2 is an alkyl group having a carbon number of 1 6, R 1 and R 2 is a large alkyl group carbon number than the same whether or R 1 toward the R 2, .) The two esters in the compound of formula (I) are more readily hydrolyzed when the ester on the carbon atom to which the chlorine atom is attached and when the two esters are trans are more easily hydrolyzed. Utilizing it enables selective production. [Selection diagram] None
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