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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-30
filingDate 2002-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55c6fe21c4e30d6fee178420d63e4765
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcdc1064a23e2da12635b0fbccc3f811
publicationDate 2004-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004059472-A
titleOfInvention Method for producing optically active 2-amino-2-phenylethanols and intermediates thereof
abstract An industrially advantageous general formula (2) (In the formula, R 1 and R 2 are the same or different and each represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, or the like.) A method for producing optically active 2-amino-2-phenylethanols represented by the formula: SOLUTION: General formula (1) (In the formula, R 1 and R 2 represent the same meaning as described above.) Is reacted in a solvent with an optically active 2-amino-2-phenylethanol represented by the general formula (2) and an optically active mandelic acid. Forming a diastereomer salt of, separating one diastereomer salt of the diastereomer salts from the other diastereomer salt, and then subjecting the separated diastereomer salt to alkali treatment. For producing optically active 2-amino-2-phenylethanols. [Selection diagram] None
priorityDate 2002-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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