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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5d9f3ca41550d315642580237250c5b0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-44
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-44
filingDate 1979-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_367d81eef2bd97fc84eebf4d9c3430b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ddce72eb4f56c7f8b24d9a22b42f09d7
publicationDate 1980-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4225726-A
titleOfInvention Catalytic condensation of aldehydes to 1,3-glycol monoesters
abstract This invention relates to an improved method for the catalyzed condensation of aldehydes in the liquid phase to form 1,3-glycol monoesters utilizing tin metal or a tin oxide catalyst. Condensation can be visualized as an aldol condensation followed by a Tischenko reaction between the aldol and a third molecule of aldehyde. In its simplest form the condensation can be illustrated by the following general formula ##STR1## R or R 1 =Hydrogen or alkyl group of 1 to 20 carbon atoms or aromatic groups. R and R 1 can also be part of a cyclic system.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001114711-A
priorityDate 1979-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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