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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_21a39b3e9cbd64f50e4548ff455b6e89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8fb9f44db08d1c42a53f3d28eaae416f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-573
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C53-126
filingDate 1998-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc8bb24bba3f7d824339d60c9d86fb07
publicationDate 2000-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000086576-A
titleOfInvention Method for producing fatty acid anhydride
abstract PROBLEM TO BE SOLVED: To provide an industrially easy and inexpensive method for producing a fatty acid anhydride with as little excess of a lower fatty acid anhydride as possible, without using an azeotropic solvent or the like. SOLUTION: The fatty acid (specific example: octanoic acid) represented by the general formula (1) R 1 CO 2 H (1) and the fatty acid represented by the general formula (2) R 2 CO—O—COR 2 (2) Lower fatty acid anhydrides (specific examples: acetic anhydride) To produce a fatty acid anhydride (specific example: octanoic anhydride) represented by the general formula (3) R 1 CO—O—COR 1 (3). 4) The above-mentioned general formula (3), wherein the lower fatty acid (specific example: acetic acid) represented by R 2 CO 2 H (4) is reacted while being removed from the reaction system by a plurality of stages of degeneration. )).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20170123355-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013532641-A
priorityDate 1998-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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