http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11292819-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-74
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-603
filingDate 1999-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f435be14edcf7d3ceb9ca458b298d4e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3c334e45df58ac124a42e1c2f74f5e1
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publicationDate 1999-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11292819-A
titleOfInvention Method for producing 2,5,6-trimethyl-2-cyclohexen-1-one
abstract PROBLEM TO BE SOLVED: To provide a method for producing 2,5,6-trimethyl-2-cyclohexen-1-one with better yield and better space-time yield on an industrial scale. In the presence of basic drugs, at elevated temperatures, 1 mol of crotonaldehyde or 1 mol of the compound to be converted to crotonaldehyde under the reaction conditions, about 5 to 30 mol of diethyl ketone and a solution or suspension of a strong base are passed through a separate conduit or at least partially in a suitable mixture A strong mixing in the form of is ensured, optionally simultaneously pumping into a heated pressure vessel, the reaction temperature being between 150 ° C. and 350 ° C., the average residence time in the pressure vessel being about 0.1 second -20 minutes, a method for producing 2,5,6-trimethyl-2-cyclohex-1-one.
priorityDate 1998-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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