http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0380783-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-59
filingDate 1989-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6bef8d9188f575b6da51eee3fa81006
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a90b8132ec70f8104ef7a0278e81ee1
publicationDate 1990-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0380783-A2
titleOfInvention Method for the preparation of 5-chloro-pentan-2-one
abstract It was an object of the invention to develop a simple and environmentally friendly process for the preparation of 5-chloropentanone-2, starting from a ketal of a levulinic acid ester, its hydrogenation and subsequent reaction with hydrochloric acid.n n n The solution is that the ketal of the levulinic acid ester is first purified by distillation, the hydrogenation catalysts for the ketal are made alkaline and the 3- (2-methyl-1,3-dioxolan-2-yl) propane-1- ol is reacted with hydrochloric acid to form 5-chloropentanone-2.n n n Use as a pharmaceutical intermediate and for the production of cyclopropyl methyl ketone.
priorityDate 1989-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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