http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01313472-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-54
filingDate 1988-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c74356eadc9f0b5e2134f0aae158e59d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03c75f61393d10bd18d5d6837ef2e639
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publicationDate 1989-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01313472-A
titleOfInvention Production of alpha-aminoacetonitriles
abstract PURPOSE: To easily obtain the subject compound useful as a fungicide, herbicide, etc., without causing the problems of solvent removal, etc., by reacting cyanhydrins derived from aldehydes and hydrogen cyanide directly with ammonia in acetonitrile without using specific reaction reagent. n CONSTITUTION: A cyanhydrin compound of formula II is produced by reacting an aldehyde of formula I (R and R 1 are H, halogen or 1-4C lower alkyl; X is O or S) with halogen cyanide without using a solvent or in a solvent in the presence of a catalyst such as triethylamine at 0-20°C. The obtained compound of formula II is made to react with ammonia in acetonitrile at 20-80°C, preferably 40-60°C to obtain the objective compound of formula III. The amount of acetonitrile is 0.1-2 liter, preferably 0.25-1.2 liter per 1mol of the cyanhydrin compound and that of ammonia is 1-20mol, especially 1-10mol. n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1988-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 24.