http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1281739-C

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1986-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b65e3e49baaad67aadc488e8758e757
publicationDate 1991-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1281739-C
titleOfInvention Method to convert primary alkanols to their corresponding esters
abstract ABSTRACT This invention is a method for converting primary alkanols to their corresponding alkanoate esters. Tile reaction of this method involves the regulation of the mole feed ratio of hydrogen gas to alkanol in the reaction zone of a copper chromite containing catalyst. The mole feed ratio of hydrogen gas is used to control the equilibrium of the reaction so as to optimize the reaction of the intermediate aldehyde to form the desired alkanoate ester. This invention can include an azeotropic distillation step wherein the desired alkanoate ester is further purified and anhydrous alkanol is recycled to be used again as alkanol reed solution. The use of an azeotropic distillation step and the recycling of the distilled alkanol permits the use with the method of this invention of an aqueous alkanol reed solutions.
priorityDate 1985-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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