Preparation method of 4-isopropenylphenol

The invention discloses a preparation method of 4-isopropenylphenol, which comprises the following steps: firstly, carrying out reaction on p-hydroxyacetophenone and 3, 4-dihydropyran to generate 1-(4-tetrahydropyran-2-oxyphenyl) ethanone; the preparation method comprises the following steps: firstl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: WANG CHENJUN, LIU HAO, CAI WENGANG, HOU XIUZE, LI TAO
Format: Patent
Sprache:chi ; 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 WANG CHENJUN
LIU HAO
CAI WENGANG
HOU XIUZE
LI TAO
description The invention discloses a preparation method of 4-isopropenylphenol, which comprises the following steps: firstly, carrying out reaction on p-hydroxyacetophenone and 3, 4-dihydropyran to generate 1-(4-tetrahydropyran-2-oxyphenyl) ethanone; the preparation method comprises the following steps: firstly, reacting methyltriphenylphosphonium bromide with potassium tert-butoxide to prepare a phosphorus ylide reagent, and then reacting 1-(4-tetrahydropyran-2-oxyphenyl) ethanone with the phosphorus ylide reagent to generate 2-(4-(1-propylene-2-yl) phenoxyl) tetrahydro-2H-pyran; finally, the 2-(4-(1-propylene-2-yl) phenoxy) tetrahydro-2H-pyran is subjected to deprotection, and the 4-isopropenyl phenol is obtained. According to the preparation method disclosed by the invention, each step of reaction is relatively clean, no obvious side reaction exists, the process pollution is small, each step of reaction condition is mild, the operation is simple and safe, the post-treatment flow is simple, the raw materials are simpl
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN118993849A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN118993849A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN118993849A3</originalsourceid><addsrcrecordid>eNrjZNAMKEotSCxKLMnMz1PITS3JyE9RyE9TMNHNLM4vKMovSM2rzCnISM3Lz-FhYE1LzClO5YXS3AyKbq4hzh66qQX58anFBYnJqXmpJfHOfoaGFpaWxhYmlo7GxKgBACDHKR4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Preparation method of 4-isopropenylphenol</title><source>esp@cenet</source><creator>WANG CHENJUN ; LIU HAO ; CAI WENGANG ; HOU XIUZE ; LI TAO</creator><creatorcontrib>WANG CHENJUN ; LIU HAO ; CAI WENGANG ; HOU XIUZE ; LI TAO</creatorcontrib><description>The invention discloses a preparation method of 4-isopropenylphenol, which comprises the following steps: firstly, carrying out reaction on p-hydroxyacetophenone and 3, 4-dihydropyran to generate 1-(4-tetrahydropyran-2-oxyphenyl) ethanone; the preparation method comprises the following steps: firstly, reacting methyltriphenylphosphonium bromide with potassium tert-butoxide to prepare a phosphorus ylide reagent, and then reacting 1-(4-tetrahydropyran-2-oxyphenyl) ethanone with the phosphorus ylide reagent to generate 2-(4-(1-propylene-2-yl) phenoxyl) tetrahydro-2H-pyran; finally, the 2-(4-(1-propylene-2-yl) phenoxy) tetrahydro-2H-pyran is subjected to deprotection, and the 4-isopropenyl phenol is obtained. According to the preparation method disclosed by the invention, each step of reaction is relatively clean, no obvious side reaction exists, the process pollution is small, each step of reaction condition is mild, the operation is simple and safe, the post-treatment flow is simple, the raw materials are simpl</description><language>chi ; eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2024</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=20241122&amp;DB=EPODOC&amp;CC=CN&amp;NR=118993849A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76516</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20241122&amp;DB=EPODOC&amp;CC=CN&amp;NR=118993849A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WANG CHENJUN</creatorcontrib><creatorcontrib>LIU HAO</creatorcontrib><creatorcontrib>CAI WENGANG</creatorcontrib><creatorcontrib>HOU XIUZE</creatorcontrib><creatorcontrib>LI TAO</creatorcontrib><title>Preparation method of 4-isopropenylphenol</title><description>The invention discloses a preparation method of 4-isopropenylphenol, which comprises the following steps: firstly, carrying out reaction on p-hydroxyacetophenone and 3, 4-dihydropyran to generate 1-(4-tetrahydropyran-2-oxyphenyl) ethanone; the preparation method comprises the following steps: firstly, reacting methyltriphenylphosphonium bromide with potassium tert-butoxide to prepare a phosphorus ylide reagent, and then reacting 1-(4-tetrahydropyran-2-oxyphenyl) ethanone with the phosphorus ylide reagent to generate 2-(4-(1-propylene-2-yl) phenoxyl) tetrahydro-2H-pyran; finally, the 2-(4-(1-propylene-2-yl) phenoxy) tetrahydro-2H-pyran is subjected to deprotection, and the 4-isopropenyl phenol is obtained. According to the preparation method disclosed by the invention, each step of reaction is relatively clean, no obvious side reaction exists, the process pollution is small, each step of reaction condition is mild, the operation is simple and safe, the post-treatment flow is simple, the raw materials are simpl</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2024</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNAMKEotSCxKLMnMz1PITS3JyE9RyE9TMNHNLM4vKMovSM2rzCnISM3Lz-FhYE1LzClO5YXS3AyKbq4hzh66qQX58anFBYnJqXmpJfHOfoaGFpaWxhYmlo7GxKgBACDHKR4</recordid><startdate>20241122</startdate><enddate>20241122</enddate><creator>WANG CHENJUN</creator><creator>LIU HAO</creator><creator>CAI WENGANG</creator><creator>HOU XIUZE</creator><creator>LI TAO</creator><scope>EVB</scope></search><sort><creationdate>20241122</creationdate><title>Preparation method of 4-isopropenylphenol</title><author>WANG CHENJUN ; LIU HAO ; CAI WENGANG ; HOU XIUZE ; LI TAO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN118993849A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2024</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>WANG CHENJUN</creatorcontrib><creatorcontrib>LIU HAO</creatorcontrib><creatorcontrib>CAI WENGANG</creatorcontrib><creatorcontrib>HOU XIUZE</creatorcontrib><creatorcontrib>LI TAO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WANG CHENJUN</au><au>LIU HAO</au><au>CAI WENGANG</au><au>HOU XIUZE</au><au>LI TAO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Preparation method of 4-isopropenylphenol</title><date>2024-11-22</date><risdate>2024</risdate><abstract>The invention discloses a preparation method of 4-isopropenylphenol, which comprises the following steps: firstly, carrying out reaction on p-hydroxyacetophenone and 3, 4-dihydropyran to generate 1-(4-tetrahydropyran-2-oxyphenyl) ethanone; the preparation method comprises the following steps: firstly, reacting methyltriphenylphosphonium bromide with potassium tert-butoxide to prepare a phosphorus ylide reagent, and then reacting 1-(4-tetrahydropyran-2-oxyphenyl) ethanone with the phosphorus ylide reagent to generate 2-(4-(1-propylene-2-yl) phenoxyl) tetrahydro-2H-pyran; finally, the 2-(4-(1-propylene-2-yl) phenoxy) tetrahydro-2H-pyran is subjected to deprotection, and the 4-isopropenyl phenol is obtained. According to the preparation method disclosed by the invention, each step of reaction is relatively clean, no obvious side reaction exists, the process pollution is small, each step of reaction condition is mild, the operation is simple and safe, the post-treatment flow is simple, the raw materials are simpl</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language chi ; eng
recordid cdi_epo_espacenet_CN118993849A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title Preparation method of 4-isopropenylphenol
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T16%3A47%3A42IST&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=WANG%20CHENJUN&rft.date=2024-11-22&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN118993849A%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