http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2557790-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D227-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C25B3-23
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D227-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C25B3-23
filingDate 1975-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9f36091965a763c8e53d393312dbe06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fd666eb36f7b33311aff38931b75f2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4ef47a432c0d1f2a4551ae766ea5ff1
publicationDate 1977-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2557790-A1
titleOfInvention PROCESS FOR THE PREPARATION OF ALCOXY DERIVATIVES FROM N-ACYLATED CYCLIC AMINES
abstract New alkoxylated heterocyclic amides are of formula (I): In the formula R1 is H, 1-8C alkyl, 6-10C aryl, 1-4C alkoxy, aralkoxy or aryloxy; R2 is 1-4C alkylene; X is 1-4C alkoxy; and Y is H, 1-4C alkoxy; and Y is H, 1-4C alkoxy or 1-4C alkoxy, but cannot be H when R1 s alkoxy. Cpds. (I) can be prepd. by electrolysis of heterocyclic amides of formula (II) with a 1-4C alkanol in the presence of an alkali metal or tetraalkylammonium tetrafluoroborate hexafluorophosphate or nitrate, pref. at 0-60 degrees C using 4-5 Faradays per mole of (II): (where Y' is H, 1-4C alkyl or 1-4C alkoxy). Cpds. (I) are fungicides and intermediates for plant-protection agents and pharmaceuticals. They can be converted tion alpha, omega-diamino carboxylic acids and trimeric DELTA'-piperidines and 1-pyrroline (inters. for anticoagulants). In an example, 1-formyl-2-methoxypiperidine is prepd. by electrochemical alkoxylation of N-formylpiperidine with MEOH.
priorityDate 1975-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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