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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e21e00e9ac38025021a2ef6901271081
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f9ba304908c7187b486482f16a0f6158
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-22
filingDate 1997-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_535f8e0a40bcaae14ddcb039e5328cb4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_528aefaff490c61f4f7a8e9f84171247
publicationDate 1998-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9811087-A1
titleOfInvention Process for preparing 1,3-dioxolane-4-methanol compounds
abstract A process for preparing 1,3-dioxolane-4-methanol compounds in a racemic modification form or an optically active form having a high purity in a high yield in a simple and cost-effective manner. The process comprises allowing an alkali (earth) metal salt of an alcohol or a carboxylic acid to act on a 4-halogenomethyl-1,3-dioxolane, prepared by acetalating a halogeno-1,2-propanediol represented by formula (1) (wherein X represents a halogen atom) in the presence of an acid catalyst, to conduct esterification or etherification and hydrolyzing the ester group and hydrogenolyzing the ether group to prepare a 1,3-dioxolane-4-methanol compound represented by formula (2) (wherein R?1 and R2¿ represent each hydrogen, an alkyl group having 1 to 4 carbon atoms, or a phenyl group, or R?1 and R2¿ together with the adjacent carbon atom may form a three- to six-membered ring.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002363134-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4601861-B2
priorityDate 1996-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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