http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4945180-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-377
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-377
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-08
filingDate 1988-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92d43a63991d90314ed573196bfa4be1
publicationDate 1990-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4945180-A
titleOfInvention Process for the preparation of E-2-propyl-2-pentenoic acid and physiologically compatible salts thereof
abstract A novel process for the preparation of E-2-propyl-2-pentenoic acid and its physiologically compatible salts is described, in which di-n-propyl-ketone-cyanohydrin is used as the starting compound. The compound is either n (a) dehydrated with thionyl chloride and the acid nitrile formed is subsequently saponified with a stoichiometric excess of potassium hydroxide, or n (b) is initially converted into 2-hydroxy-2-propyl-pentanoic acid and the latter is subsequently dehydrated in the presence of a less than stoichiometric quantity of a tertiary amine at a temperature of at least 200° C. n The free acid is optionally converted into the salt form, preferably using the corresponding salts of carbon dioxide in an aqueous acetone solution.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6864389-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006223888-A1
priorityDate 1987-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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