AMINATION OF DIHYDRIC PHENOL

PURPOSE:To obtain the subject compound on an industrial scale in high yield by using a phenolic compound and a metal phosphate in the amination of the hydroxyl group of a dihydric phenol to produce the corresponding aminophenols and phenylenediamines. CONSTITUTION:Aminophenols and phenylenediamines...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: NAGANUMA YOSHITARO, WATABE YASUYOSHI, SUGIYAMA EIICHI, KOMIYAMA TADASHI
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 NAGANUMA YOSHITARO
WATABE YASUYOSHI
SUGIYAMA EIICHI
KOMIYAMA TADASHI
description PURPOSE:To obtain the subject compound on an industrial scale in high yield by using a phenolic compound and a metal phosphate in the amination of the hydroxyl group of a dihydric phenol to produce the corresponding aminophenols and phenylenediamines. CONSTITUTION:Aminophenols and phenylenediamines useful as raw materials for the raw material or modifier of dyes, pharmaceuticals, agricultural chemicals, rubber chemicals, synthetic resins and synthetic fibers are produced by aminating the hydroxyl group of a dihydric phenol with an amine, preferably ammonia, primary amine or secondary amine. In the above process, a phenolic compound and one or more kinds of metal phosphates selected from titanium, zirconium and hafnium phosphates are added to the reaction system to suppress the by-production of tarry substance, to proceed the reaction without losing the dihydric phenol and to obtain the objective compound in high yield.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JPH03112946A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JPH03112946A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JPH03112946A3</originalsourceid><addsrcrecordid>eNrjZJBx9PX0cwzx9PdT8HdTcPH0iHQJ8nRWCPBw9fP34WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BHgbGhoZGliZmjsbEqAEAbKAg5A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>AMINATION OF DIHYDRIC PHENOL</title><source>esp@cenet</source><creator>NAGANUMA YOSHITARO ; WATABE YASUYOSHI ; SUGIYAMA EIICHI ; KOMIYAMA TADASHI</creator><creatorcontrib>NAGANUMA YOSHITARO ; WATABE YASUYOSHI ; SUGIYAMA EIICHI ; KOMIYAMA TADASHI</creatorcontrib><description>PURPOSE:To obtain the subject compound on an industrial scale in high yield by using a phenolic compound and a metal phosphate in the amination of the hydroxyl group of a dihydric phenol to produce the corresponding aminophenols and phenylenediamines. CONSTITUTION:Aminophenols and phenylenediamines useful as raw materials for the raw material or modifier of dyes, pharmaceuticals, agricultural chemicals, rubber chemicals, synthetic resins and synthetic fibers are produced by aminating the hydroxyl group of a dihydric phenol with an amine, preferably ammonia, primary amine or secondary amine. In the above process, a phenolic compound and one or more kinds of metal phosphates selected from titanium, zirconium and hafnium phosphates are added to the reaction system to suppress the by-production of tarry substance, to proceed the reaction without losing the dihydric phenol and to obtain the objective compound in high yield.</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=19910514&amp;DB=EPODOC&amp;CC=JP&amp;NR=H03112946A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19910514&amp;DB=EPODOC&amp;CC=JP&amp;NR=H03112946A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAGANUMA YOSHITARO</creatorcontrib><creatorcontrib>WATABE YASUYOSHI</creatorcontrib><creatorcontrib>SUGIYAMA EIICHI</creatorcontrib><creatorcontrib>KOMIYAMA TADASHI</creatorcontrib><title>AMINATION OF DIHYDRIC PHENOL</title><description>PURPOSE:To obtain the subject compound on an industrial scale in high yield by using a phenolic compound and a metal phosphate in the amination of the hydroxyl group of a dihydric phenol to produce the corresponding aminophenols and phenylenediamines. CONSTITUTION:Aminophenols and phenylenediamines useful as raw materials for the raw material or modifier of dyes, pharmaceuticals, agricultural chemicals, rubber chemicals, synthetic resins and synthetic fibers are produced by aminating the hydroxyl group of a dihydric phenol with an amine, preferably ammonia, primary amine or secondary amine. In the above process, a phenolic compound and one or more kinds of metal phosphates selected from titanium, zirconium and hafnium phosphates are added to the reaction system to suppress the by-production of tarry substance, to proceed the reaction without losing the dihydric phenol and to obtain the objective compound in high yield.</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>eNrjZJBx9PX0cwzx9PdT8HdTcPH0iHQJ8nRWCPBw9fP34WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BHgbGhoZGliZmjsbEqAEAbKAg5A</recordid><startdate>19910514</startdate><enddate>19910514</enddate><creator>NAGANUMA YOSHITARO</creator><creator>WATABE YASUYOSHI</creator><creator>SUGIYAMA EIICHI</creator><creator>KOMIYAMA TADASHI</creator><scope>EVB</scope></search><sort><creationdate>19910514</creationdate><title>AMINATION OF DIHYDRIC PHENOL</title><author>NAGANUMA YOSHITARO ; WATABE YASUYOSHI ; SUGIYAMA EIICHI ; KOMIYAMA TADASHI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPH03112946A3</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>NAGANUMA YOSHITARO</creatorcontrib><creatorcontrib>WATABE YASUYOSHI</creatorcontrib><creatorcontrib>SUGIYAMA EIICHI</creatorcontrib><creatorcontrib>KOMIYAMA TADASHI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAGANUMA YOSHITARO</au><au>WATABE YASUYOSHI</au><au>SUGIYAMA EIICHI</au><au>KOMIYAMA TADASHI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>AMINATION OF DIHYDRIC PHENOL</title><date>1991-05-14</date><risdate>1991</risdate><abstract>PURPOSE:To obtain the subject compound on an industrial scale in high yield by using a phenolic compound and a metal phosphate in the amination of the hydroxyl group of a dihydric phenol to produce the corresponding aminophenols and phenylenediamines. CONSTITUTION:Aminophenols and phenylenediamines useful as raw materials for the raw material or modifier of dyes, pharmaceuticals, agricultural chemicals, rubber chemicals, synthetic resins and synthetic fibers are produced by aminating the hydroxyl group of a dihydric phenol with an amine, preferably ammonia, primary amine or secondary amine. In the above process, a phenolic compound and one or more kinds of metal phosphates selected from titanium, zirconium and hafnium phosphates are added to the reaction system to suppress the by-production of tarry substance, to proceed the reaction without losing the dihydric phenol and to obtain the objective compound in high yield.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_JPH03112946A
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 AMINATION OF DIHYDRIC PHENOL
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T03%3A38%3A25IST&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=NAGANUMA%20YOSHITARO&rft.date=1991-05-14&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJPH03112946A%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