http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03232828-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C25-13
filingDate 1990-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8cfb7c4bf9f283054043056afc0fdc45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92d510a9e900f5b9710e51894036fa9f
publicationDate 1991-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03232828-A
titleOfInvention Production of 1,2-difluorobenzene
abstract PURPOSE: To obtain the subject substance in high yield by diazotizing 2- fluoroaniline, converting to a borofluoride and thermally decomposing the resultant 2-fluorobenzene diazonium tetrafluoroborate in a polychlorinated aromatic solvent. n CONSTITUTION: 2-Fluoroaniline is diazotized with sodium nitrite, etc., in the presence of a mineral acid, the precipitated inorganic salt is removed by filtration and the product is made to react with hydroborofluoric acid to obtain 2-fluorobenzene diazonium tetrafluoroborate in the form of slurry. The slurry is filtered and the obtained powder is mixed with 0.5-10 times weight of a polychlorinated aromatic solvent (e.g. 1,2-dichlorobenzene) without drying. The mixture is heated at ≤90°C under reduced pressure to distill off water. When the system is returned to normal pressure, the decomposition takes place at about 155°C and the distilled and purified subject substance is continuously taken out of the system. The compound is useful as an intermediate raw material for pharmaceuticals, agricultural chemicals liquid crystal materials, etc. n COPYRIGHT: (C)1991,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114874067-A
priorityDate 1990-02-06-04:00^^<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: 27.