http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S60123462-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C313-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-02
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filingDate 1983-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ced89da836b5b0521e7a017597861b27
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publicationDate 1985-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60123462-A
titleOfInvention Production of aminoalkanethiol
abstract PURPOSE: To obtain the titled compound useful as a raw material for heterocyclic compounds useful as agricultural chemicals and medicines, etc. in high yield, by reacting an aminoalkyl halide hydrohalide with hydrogen sulfide and ammonia in a solvent. n CONSTITUTION: An aminoalkyl halide hydrohalide expressed by formula I (X 1 and X 2 are halogen; n is an integer 2W6; R 1 and R 2 are 1W12C alkyl or 4W12C cycloalkyl, etc.) is reacted with hydrogen sulfide and ammonia in a solvent, e.g. methanol, to give an aminoalkanethiol hydrohalide expressed by formula II, which is then neutralized with a base, e.g. NaOH, to afford the aimed aminoalkanethiol expressed by formula III. The reaction is usually carried out at 50W 200°C, preferably 80W150°C for 0.5W10hr. Any form of ammonia gas, liquid ammonia or aqueous solution of ammonia is effective for the ammonia. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1983-12-06-04:00^^<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: 25.