http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-476919-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_38214d2b61566e8b243556d174e623c6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-277
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1979-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1979-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-476919-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF NEW 2-PIRROLIDONE COMPOUNDS.
abstract Process for preparing the 4-amino-hex-5-ynoic salt or a salt thereof, characterized in that it consists in treating a pyrrolidone compound of the formula **formula** where R1 is hydroxy, amino or tertiary butoxy, with a strong base in a lower alcohol solvent at a temperature of about 20°C, to the reflux temperature of the solvent for about 6 to 24 hours when R1 is amino, decarboxylate the 3-carboxy derivative or its tertiary butyl ester to provide 5-vinyl-2-pyrrolidone being treated in a chlorinated hydrocarbon solvent to acetic acid with an equivalent amount of bromine at a temperature of about 4 to 24 hours, treating the dibromo intermediate thus formed in an ether solvent or liquid ammonia with a strong base for about 1 to 40 hours at a temperature of about -80° to 125°C and quench rapidly with water followed by acid hydrolysis and when desired the free base is subjected to subsequent treatment with a base.
priorityDate 1978-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 23.