PRODUCTION OF DIFLUORONITROANILINE

PURPOSE:To obtain the subject compound useful as an intermediate for precise chemicals such as agricultural chemicals, medicines or dyes in good yield by reacting 2,4-difluoroaniline with nitric acids. CONSTITUTION:2,4-Difluoroaniline is allowed to react with nitric acids such as nitric acid, fuming...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: NASU RIKUO, HAMAGUCHI MOTOHIKO
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator NASU RIKUO
HAMAGUCHI MOTOHIKO
description PURPOSE:To obtain the subject compound useful as an intermediate for precise chemicals such as agricultural chemicals, medicines or dyes in good yield by reacting 2,4-difluoroaniline with nitric acids. CONSTITUTION:2,4-Difluoroaniline is allowed to react with nitric acids such as nitric acid, fuming nitric acid or mixed acid of concentrated nitric acid and concentrated sulfuric acid in an amount of 0.9-1.5mol, preferably 0.95-1.05mol based on 1mol 2,4-difluoroaniline to afford the objective compound. The aforementioned reaction is preferably carried out at -10 to -30 deg.C temperature for 0.5-2 hr. Furthermore, urea in an amount of 0.05-0.30mol, preferably 0.10-0.20mol, based on 1 mol raw material compound is present to remarkably improve the production ratio of the objective compound.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JPH03255056A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JPH03255056A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JPH03255056A3</originalsourceid><addsrcrecordid>eNrjZFAKCPJ3CXUO8fT3U_B3U3DxdPMJ9Q_y9_MMCfJ39PP08fRz5WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BHgbGRqamBqZmjsbEqAEAZ48jCw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>PRODUCTION OF DIFLUORONITROANILINE</title><source>esp@cenet</source><creator>NASU RIKUO ; HAMAGUCHI MOTOHIKO</creator><creatorcontrib>NASU RIKUO ; HAMAGUCHI MOTOHIKO</creatorcontrib><description>PURPOSE:To obtain the subject compound useful as an intermediate for precise chemicals such as agricultural chemicals, medicines or dyes in good yield by reacting 2,4-difluoroaniline with nitric acids. CONSTITUTION:2,4-Difluoroaniline is allowed to react with nitric acids such as nitric acid, fuming nitric acid or mixed acid of concentrated nitric acid and concentrated sulfuric acid in an amount of 0.9-1.5mol, preferably 0.95-1.05mol based on 1mol 2,4-difluoroaniline to afford the objective compound. The aforementioned reaction is preferably carried out at -10 to -30 deg.C temperature for 0.5-2 hr. Furthermore, urea in an amount of 0.05-0.30mol, preferably 0.10-0.20mol, based on 1 mol raw material compound is present to remarkably improve the production ratio of the objective compound.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; APPARATUS THEREFOR ; CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY ; CHEMISTRY ; GENERAL METHODS OF ORGANIC CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY ; PERFORMING OPERATIONS ; PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL ; THEIR RELEVANT APPARATUS ; TRANSPORTING</subject><creationdate>1991</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&amp;date=19911113&amp;DB=EPODOC&amp;CC=JP&amp;NR=H03255056A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19911113&amp;DB=EPODOC&amp;CC=JP&amp;NR=H03255056A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NASU RIKUO</creatorcontrib><creatorcontrib>HAMAGUCHI MOTOHIKO</creatorcontrib><title>PRODUCTION OF DIFLUORONITROANILINE</title><description>PURPOSE:To obtain the subject compound useful as an intermediate for precise chemicals such as agricultural chemicals, medicines or dyes in good yield by reacting 2,4-difluoroaniline with nitric acids. CONSTITUTION:2,4-Difluoroaniline is allowed to react with nitric acids such as nitric acid, fuming nitric acid or mixed acid of concentrated nitric acid and concentrated sulfuric acid in an amount of 0.9-1.5mol, preferably 0.95-1.05mol based on 1mol 2,4-difluoroaniline to afford the objective compound. The aforementioned reaction is preferably carried out at -10 to -30 deg.C temperature for 0.5-2 hr. Furthermore, urea in an amount of 0.05-0.30mol, preferably 0.10-0.20mol, based on 1 mol raw material compound is present to remarkably improve the production ratio of the objective compound.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>APPARATUS THEREFOR</subject><subject>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>GENERAL METHODS OF ORGANIC CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PERFORMING OPERATIONS</subject><subject>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</subject><subject>THEIR RELEVANT APPARATUS</subject><subject>TRANSPORTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1991</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFAKCPJ3CXUO8fT3U_B3U3DxdPMJ9Q_y9_MMCfJ39PP08fRz5WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BHgbGRqamBqZmjsbEqAEAZ48jCw</recordid><startdate>19911113</startdate><enddate>19911113</enddate><creator>NASU RIKUO</creator><creator>HAMAGUCHI MOTOHIKO</creator><scope>EVB</scope></search><sort><creationdate>19911113</creationdate><title>PRODUCTION OF DIFLUORONITROANILINE</title><author>NASU RIKUO ; HAMAGUCHI MOTOHIKO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPH03255056A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1991</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>APPARATUS THEREFOR</topic><topic>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>GENERAL METHODS OF ORGANIC CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PERFORMING OPERATIONS</topic><topic>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</topic><topic>THEIR RELEVANT APPARATUS</topic><topic>TRANSPORTING</topic><toplevel>online_resources</toplevel><creatorcontrib>NASU RIKUO</creatorcontrib><creatorcontrib>HAMAGUCHI MOTOHIKO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NASU RIKUO</au><au>HAMAGUCHI MOTOHIKO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PRODUCTION OF DIFLUORONITROANILINE</title><date>1991-11-13</date><risdate>1991</risdate><abstract>PURPOSE:To obtain the subject compound useful as an intermediate for precise chemicals such as agricultural chemicals, medicines or dyes in good yield by reacting 2,4-difluoroaniline with nitric acids. CONSTITUTION:2,4-Difluoroaniline is allowed to react with nitric acids such as nitric acid, fuming nitric acid or mixed acid of concentrated nitric acid and concentrated sulfuric acid in an amount of 0.9-1.5mol, preferably 0.95-1.05mol based on 1mol 2,4-difluoroaniline to afford the objective compound. The aforementioned reaction is preferably carried out at -10 to -30 deg.C temperature for 0.5-2 hr. Furthermore, urea in an amount of 0.05-0.30mol, preferably 0.10-0.20mol, based on 1 mol raw material compound is present to remarkably improve the production ratio of the objective compound.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_JPH03255056A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
APPARATUS THEREFOR
CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY
CHEMISTRY
GENERAL METHODS OF ORGANIC CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
THEIR RELEVANT APPARATUS
TRANSPORTING
title PRODUCTION OF DIFLUORONITROANILINE
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T06%3A44%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=NASU%20RIKUO&rft.date=1991-11-13&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJPH03255056A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true