NOVEL METHOD FOR PREPARING O-DIFLUOROBENZENE
PURPOSE:To prepare the titled compound useful as a synthetic intermediate for antimicrobial agents in high yield, by adding a small amount of a silicone oil to 2-fluoro-1-benzenediazonium tetrafluoroborate in the thermal decomposition thereof. CONSTITUTION:o-Fluoroaniline is diazotized and then reac...
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creator | INAKA YUTAKA OOTSUBO JIYUNICHIROU KANOU MASANOBU |
description | PURPOSE:To prepare the titled compound useful as a synthetic intermediate for antimicrobial agents in high yield, by adding a small amount of a silicone oil to 2-fluoro-1-benzenediazonium tetrafluoroborate in the thermal decomposition thereof. CONSTITUTION:o-Fluoroaniline is diazotized and then reacted with a fluoronating agent, e.g. borofluoric acid to give 2-fluoro-1-benzenediazonium tetrafluoroborate. A small amount, preferably about 4-5wt% based on the above-mentioned raw material, of a silicone oil is added to the 2-fluoro-1-benzenediazonium tetrafluoroborate and decomposed thermally under heating at 100- 180 deg.C, preferably 130-160 deg.C, for about 1-5hr to afford the aimed o-difluorobenzene. EFFECT:The reaction proceeds very mildly, and a reaction vessel of relatively small volume is enough. |
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CONSTITUTION:o-Fluoroaniline is diazotized and then reacted with a fluoronating agent, e.g. borofluoric acid to give 2-fluoro-1-benzenediazonium tetrafluoroborate. A small amount, preferably about 4-5wt% based on the above-mentioned raw material, of a silicone oil is added to the 2-fluoro-1-benzenediazonium tetrafluoroborate and decomposed thermally under heating at 100- 180 deg.C, preferably 130-160 deg.C, for about 1-5hr to afford the aimed o-difluorobenzene. EFFECT:The reaction proceeds very mildly, and a reaction vessel of relatively small volume is enough.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1984</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19840416&DB=EPODOC&CC=JP&NR=S5967232A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19840416&DB=EPODOC&CC=JP&NR=S5967232A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>INAKA YUTAKA</creatorcontrib><creatorcontrib>OOTSUBO JIYUNICHIROU</creatorcontrib><creatorcontrib>KANOU MASANOBU</creatorcontrib><title>NOVEL METHOD FOR PREPARING O-DIFLUOROBENZENE</title><description>PURPOSE:To prepare the titled compound useful as a synthetic intermediate for antimicrobial agents in high yield, by adding a small amount of a silicone oil to 2-fluoro-1-benzenediazonium tetrafluoroborate in the thermal decomposition thereof. CONSTITUTION:o-Fluoroaniline is diazotized and then reacted with a fluoronating agent, e.g. borofluoric acid to give 2-fluoro-1-benzenediazonium tetrafluoroborate. A small amount, preferably about 4-5wt% based on the above-mentioned raw material, of a silicone oil is added to the 2-fluoro-1-benzenediazonium tetrafluoroborate and decomposed thermally under heating at 100- 180 deg.C, preferably 130-160 deg.C, for about 1-5hr to afford the aimed o-difluorobenzene. 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CONSTITUTION:o-Fluoroaniline is diazotized and then reacted with a fluoronating agent, e.g. borofluoric acid to give 2-fluoro-1-benzenediazonium tetrafluoroborate. A small amount, preferably about 4-5wt% based on the above-mentioned raw material, of a silicone oil is added to the 2-fluoro-1-benzenediazonium tetrafluoroborate and decomposed thermally under heating at 100- 180 deg.C, preferably 130-160 deg.C, for about 1-5hr to afford the aimed o-difluorobenzene. EFFECT:The reaction proceeds very mildly, and a reaction vessel of relatively small volume is enough.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | NOVEL METHOD FOR PREPARING O-DIFLUOROBENZENE |
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