http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04178361-A

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-29
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-29
filingDate 1990-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c651b0343d67269adf7f70204ece0a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acb295f96a94f7bfc4fe6fdf60969d92
publicationDate 1992-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04178361-A
titleOfInvention Preparation of alpha-formylamino nitrile
abstract PURPOSE: To obtain the titled compound in a high yield by reacting a cyanohydrin with formamide in the presence of an acidic catalyst and an ammonium salt as a co-catalyst with minimal occurrence of side reactions. n CONSTITUTION: In the presence of an acidic catalyst (e.g. inorganic acid organic carboxylic acid, sulfonic acid, or preferably 1-6C monocarboxylic acid-in particular, formic acid) together with an ammonium salt acting as a co-catalyst (the ammonium salt of the acid used as catalyst is suited.), a compound of formula I (R 1 and R 2 is H, 1-10C (hetero) aliphatic, 3-6C (hetero) alicyclic, 7-12C araliphatic, 4-12C heteroaraliphatic, 6-10C aromatic or 3-10C heteroaromatic radicals) are reacted with a compound of formula II at a temperature of 20-150°C, more preferably 80-100°C to form a compound of formula III. To one mole of the formula I compound, 1.2-1.8 moles of the formula II compound, and 0.1-0.3 mole of the acid and of the ammonium salt are preferably used. n COPYRIGHT: (C)1992,JPO
priorityDate 1989-12-22-04:00^^<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: 22.