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filingDate 1984-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df18d82388a6ec7d8be05db2941d420a
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publicationDate 1986-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6167498-A
titleOfInvention Production of d-valine and l-valine from isopropyl hydantoin
abstract PURPOSE: To produce high-purity D-valine and L-valine, by hydrolyzing isopropyl hydantoin with an alkali, and subjecting the reaction liquid containing DL-valine to a specific treatment. n CONSTITUTION: Isopropyl hydantoin is mixed with an alkali and water, and hydrolyzed at ≤100°C. The obtained reaction liquid containing DL-valine is acetylated with acetic anhydride at 20W30°C, and N-acetyl-DL-valine is precipitated from the mixture with an acid. The N-acetyl-DL-valine is dissolved in water at a concentration of 5W40wt%, added with aminoacylase to effect the exclusive hydrolysis of the acetyl group of the N-acetyl-L-valine and obtain an acylase reaction liquid containing N-acetyl-D-valine and L-valine. The reaction liquid is adjusted to ≤1pH with an acid to effect the crystallization of N-acetyl-D- valine, which is separated by solid-liquid separation process and hydrolyzed with an acid to obtain D-valine. The acidic filtrate is made to contact with a strongly acidic ion exchange resin to effect the adsorption of L-valine, and the adsorbed L-valine is eluted. n COPYRIGHT: (C)1986,JPO&Japio
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