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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C317-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-92
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-84
filingDate 1968-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96de8d268bf592092170e82cd871cf88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cbc5a4f988c87a8fab7cecae50d2b25
publicationDate 1970-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1202166-A
titleOfInvention Process for the preparation of phthalic acid phenylether derivatives
abstract 1,202,166. Phenoxyphthalic acid esters. FARBENFABRIKEN BAYER A.G. 13 June, 1968 [26 July, 1967], No. 28091/68. Heading C2C. [Also in Division A5] Invention relates to phenoxyphthalic acid esters of the general formula in which R<SP>1</SP> is an electrophilic radical and R 2 and R<SP>3</SP> which may be the same or different denote aliphatic or aromatic hydrocarbon radicals. R<SP>1</SP> may be NO 2 , CN, COOR<SP>4</SP>, SO 2 R<SP>4</SP> or COR<SP>4</SP> group and R<SP>4</SP> may be alkyl or phenyl group. The compounds may be prepared by reacting an alkali metal salt or an alkaline earth metal salt of a hydroxyphthalic acid ester in a polar organic solvent at a temperature in the range of from 50‹ to 200‹ C. with a halogenated benzene derivative which is substituted by at least one electrophilic group. In an example 4-hydroxy phthalic acid was reacted with p-chloro nitro benzene to produce dimethyl ester of 4-(4<SP>1</SP>-nitrophenoxy) phthalic acid.
priorityDate 1967-07-26-04:00^^<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.