http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5721346-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-587
filingDate 1980-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e128f4705b616b1589fabdc23791575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f680019a1a3038e0fc7e226737c2f884
publicationDate 1982-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5721346-A
titleOfInvention Production of farnesylacetic ester
abstract PURPOSE: The reaction of nerolidol with a malonic diester is conducted in a specific solvent such as naphthalene, diphenyl or anisole in the presence of a catalyst amount of N-methylpyrrolidone to produce the titled substance economically in a short time, which is used to produce medicines. n CONSTITUTION: The reaction between nerolidol (3,7,11-trimethyl-1,6,10-dodecatriene-3-ol) of formula I and a malonic diester of formula II (R 1 , R 2 are alkyl) is carried out in a solvent selected from the group consisting of aromatic hydrocarbons such as naphthalene, alkyl-substituted naphthalene, diphenyl, alkyl-substituted diphenyl, and aromatic ethers such as diphenyl ether, benzyl ether, anipole, phenetole or veratrol in the presence of N-methylpyrrolidone or hexamethyl phosphoric traiamide to give compounds of formula III and formula IV. n COPYRIGHT: (C)1982,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05271258-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5574025-A
priorityDate 1980-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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