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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-34
filingDate 1988-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a37eb02b6f8feae917069cc782f5e3f7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bfe1025b17a929da32621c3f08547173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27bd69a7d6fa9bb1a7abc778dbdbfbc8
publicationDate 1990-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0217167-A
titleOfInvention Production of p-aminothiophenol
abstract PURPOSE: To readily obtain the above substance which is a raw material intermediate for medicines, engineering plastics, etc., without forming by-products by reacting a p-halogenated nitrobenzene as a starting raw material with sodium sulfide in water solvent containing a surfactant. n CONSTITUTION: A p-halogenated nitrobenzene (e.g. p-chloronitrobenzene or p-bromonitrobenzene) is used as a starting raw material and a surfactant is added into water solvent to disperse the raw material therein. Sodium sulfide is subsequently dropped (the sodium sulfide is preferably fed as an aqueous solution and the concentration thereof is 5-30wt.%, especially 15-25wt.% at 20-80°C temperature in dropping with holding time of 0.5-4hr after the dropping). Reductive reaction is then preferably carried out at 85-150°C in an inert gas atmosphere to afford the objective compound. n COPYRIGHT: (C)1990,JPO&Japio
priorityDate 1988-07-05-04:00^^<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: 27.