http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-934577-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0235f5aeeff44e5b1733138b721f5c06
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-045
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-26
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-045
filingDate 1961-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1963-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-934577-A
titleOfInvention Preparation of 3-(trifluoromethyl)-phenols
abstract A phenol having the general formula <FORM:0934577/IV(a)/1> wherein R is a hydrogen or halogen atom or an alkyl, aryl or nitro radical is prepared by diazotising 3-(trifluoromethyl)-4-R-aniline to form a corresponding diazonium salt, hydrolysing the diazonium salt with a boiling mixture of at least 100 ml. of xylene per mole of diazonium salt and aqueous copper sulphate solution containing at least 10g. of copper sulphate pentahydrate per mole of diazonium salt, and subsequently recovering the phenol. The group R is exemplified by chlorine and bromine atoms; straight or branched chain alkyl radicals having 1 to 12 carbon atoms, e.g. methyl, ethyl, propyl, butyl, hexyl, dodecyl and isobutyl radicals; phenyl, naphthyl or alkyl substituted phenyl and naphthyl radicals, e.g. p-tolyl. 3-(Trifluoromethyl)-4-nitro-aniline is prepared by hydrolysing 3-(trifluoromethyl)-4-nitro-acetanilide with a mixture of concentrated sulphuric acid and water.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-1257784-B
priorityDate 1961-04-06-04:00^^<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: 43.