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filingDate 1972-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1975-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6154a2c4e90b8a3705355fa443f87717
publicationDate 1975-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3903150-A
titleOfInvention Process for preparing 3-fluoro-D-alanine
abstract 3-Fluoro-D-analine is prepared by an asymmetric synthesis wherein fluoroacetaldehyde is reacted with D-optically active amine, such as D- Alpha -methylbenzylamine to form the corresponding acetaldimine, which is reacted with hydrogen cyanide to form D-2-(D- Alpha -methylbenzylamino)-3fluoropropionitrile, followed by hydrolysis of the nitrile and hydrogenolysis of the methylbenzyl group. Other D-optically active amines such as R(D)-phenyl-glycine and 1-amino-(S)-2-((R)1-hydroxyethyl)indoline may be employed in the above process in place of the D- Alpha -methyl-benzyl amine. The 3-fluoro-Dalanine thus obtained is a potent antibacterial agent.
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