http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114436789-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J35-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-236
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J35-10
filingDate 2022-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114436789-B
titleOfInvention A kind of green environment-friendly method for synthesizing veratraldehyde
abstract The invention provides a green and environment-friendly method for synthesizing veratraldehyde, which belongs to the technical field of perfume intermediate synthesis, and comprises the following steps: S1, adding vanillin, a methylating reagent and a catalyst to a reaction solvent, and stirring and heat-retaining reaction after heating up; Wherein, the methylating reagent is 1-methoxy-2,2,6,6-tetramethylpiperidine or 1-methoxy-4-hydroxyl-2,2,6,6-tetramethyl Piperidinol, the catalyst includes at least one of oxides, hydroxides, and carbonates of Cs or Ba; S2, after the stirring reaction is completed, wash with deionized water, collect the organic layer, and obtain after steaming the reaction solvent Veratraldehyde; the present invention simplifies the synthesis process, avoids the disadvantages of low production yield, many by-products, difficult separation and the like.
priorityDate 2022-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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