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...
Gespeichert in:
Hauptverfasser: | , , , |
---|---|
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&date=19910514&DB=EPODOC&CC=JP&NR=H03112946A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19910514&DB=EPODOC&CC=JP&NR=H03112946A$$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 |