Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes
The synthesis of 4‐formylpyrazoles using Vilsmeier‐Haack reagent is a common protocol in pyrazole chemistry. An efficient microwave‐assisted synthesis of 4‐formylpyrazoles by employing Vilsmeier‐Haack reagent (OPC‐VH) derived from phthaloyl dichloride/dimethylformamide has been described. This metho...
Gespeichert in:
Veröffentlicht in: | Journal of heterocyclic chemistry 2020-02, Vol.57 (2), p.796-804 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 804 |
---|---|
container_issue | 2 |
container_start_page | 796 |
container_title | Journal of heterocyclic chemistry |
container_volume | 57 |
creator | Kumari, Poonam Sood, Sumit Kumar, Anil Singh, Karan |
description | The synthesis of 4‐formylpyrazoles using Vilsmeier‐Haack reagent is a common protocol in pyrazole chemistry. An efficient microwave‐assisted synthesis of 4‐formylpyrazoles by employing Vilsmeier‐Haack reagent (OPC‐VH) derived from phthaloyl dichloride/dimethylformamide has been described. This method offers the advantages of operational simplicity, avoiding the use of POCl3 as toxic reagents and reuse of the by‐product in the preparation of phthaloyl dichloride. |
doi_str_mv | 10.1002/jhet.3824 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2352033472</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2352033472</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2974-235722ecb2dcba82f4e1eab8708454f8dd740f8599a992f2b83aa0e84447ac93</originalsourceid><addsrcrecordid>eNp1kM9OwzAMxiMEEmNw4A0qceLQLf-qJEc0DQoaYocJcYvc1tU6unUkHVM58Qg8I09CyrhysCzbP3-WP0IuGR0xSvl4tcR2JDSXR2TAjBRxwow4JoMw4zFL-MspOfN-FUomlBqQ-WOVu2YP7_j9-QXeV77FInquar_GCl1opgD5a-S7TbvEMI6aMpp3Dj6aul-RIXJwGdQFLrsC_Tk5KaH2ePGXh2RxO11M0nj2dHc_uZnFOTdKxlwkinPMM17kGWheSmQImVZUy0SWuiiUpKVOjAFjeMkzLQAoaimlgtyIIbk6yG5d87ZD39pVs3ObcNEGaU6FkIoH6vpAhR-9d1jaravW4DrLqO39sr1ftvcrsOMDu69q7P4H7UM6Xfxu_AA_mnF4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2352033472</pqid></control><display><type>article</type><title>Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes</title><source>Wiley Online Library</source><creator>Kumari, Poonam ; Sood, Sumit ; Kumar, Anil ; Singh, Karan</creator><creatorcontrib>Kumari, Poonam ; Sood, Sumit ; Kumar, Anil ; Singh, Karan</creatorcontrib><description>The synthesis of 4‐formylpyrazoles using Vilsmeier‐Haack reagent is a common protocol in pyrazole chemistry. An efficient microwave‐assisted synthesis of 4‐formylpyrazoles by employing Vilsmeier‐Haack reagent (OPC‐VH) derived from phthaloyl dichloride/dimethylformamide has been described. This method offers the advantages of operational simplicity, avoiding the use of POCl3 as toxic reagents and reuse of the by‐product in the preparation of phthaloyl dichloride.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.3824</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Chemical synthesis ; Dichlorides ; Organic chemistry ; Pyrazole ; Reagents</subject><ispartof>Journal of heterocyclic chemistry, 2020-02, Vol.57 (2), p.796-804</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><rights>2020 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2974-235722ecb2dcba82f4e1eab8708454f8dd740f8599a992f2b83aa0e84447ac93</citedby><cites>FETCH-LOGICAL-c2974-235722ecb2dcba82f4e1eab8708454f8dd740f8599a992f2b83aa0e84447ac93</cites><orcidid>0000-0001-8956-5558</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhet.3824$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.3824$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Kumari, Poonam</creatorcontrib><creatorcontrib>Sood, Sumit</creatorcontrib><creatorcontrib>Kumar, Anil</creatorcontrib><creatorcontrib>Singh, Karan</creatorcontrib><title>Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes</title><title>Journal of heterocyclic chemistry</title><description>The synthesis of 4‐formylpyrazoles using Vilsmeier‐Haack reagent is a common protocol in pyrazole chemistry. An efficient microwave‐assisted synthesis of 4‐formylpyrazoles by employing Vilsmeier‐Haack reagent (OPC‐VH) derived from phthaloyl dichloride/dimethylformamide has been described. This method offers the advantages of operational simplicity, avoiding the use of POCl3 as toxic reagents and reuse of the by‐product in the preparation of phthaloyl dichloride.</description><subject>Chemical synthesis</subject><subject>Dichlorides</subject><subject>Organic chemistry</subject><subject>Pyrazole</subject><subject>Reagents</subject><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kM9OwzAMxiMEEmNw4A0qceLQLf-qJEc0DQoaYocJcYvc1tU6unUkHVM58Qg8I09CyrhysCzbP3-WP0IuGR0xSvl4tcR2JDSXR2TAjBRxwow4JoMw4zFL-MspOfN-FUomlBqQ-WOVu2YP7_j9-QXeV77FInquar_GCl1opgD5a-S7TbvEMI6aMpp3Dj6aul-RIXJwGdQFLrsC_Tk5KaH2ePGXh2RxO11M0nj2dHc_uZnFOTdKxlwkinPMM17kGWheSmQImVZUy0SWuiiUpKVOjAFjeMkzLQAoaimlgtyIIbk6yG5d87ZD39pVs3ObcNEGaU6FkIoH6vpAhR-9d1jaravW4DrLqO39sr1ftvcrsOMDu69q7P4H7UM6Xfxu_AA_mnF4</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Kumari, Poonam</creator><creator>Sood, Sumit</creator><creator>Kumar, Anil</creator><creator>Singh, Karan</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-8956-5558</orcidid></search><sort><creationdate>202002</creationdate><title>Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes</title><author>Kumari, Poonam ; Sood, Sumit ; Kumar, Anil ; Singh, Karan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2974-235722ecb2dcba82f4e1eab8708454f8dd740f8599a992f2b83aa0e84447ac93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Chemical synthesis</topic><topic>Dichlorides</topic><topic>Organic chemistry</topic><topic>Pyrazole</topic><topic>Reagents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumari, Poonam</creatorcontrib><creatorcontrib>Sood, Sumit</creatorcontrib><creatorcontrib>Kumar, Anil</creatorcontrib><creatorcontrib>Singh, Karan</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumari, Poonam</au><au>Sood, Sumit</au><au>Kumar, Anil</au><au>Singh, Karan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2020-02</date><risdate>2020</risdate><volume>57</volume><issue>2</issue><spage>796</spage><epage>804</epage><pages>796-804</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>The synthesis of 4‐formylpyrazoles using Vilsmeier‐Haack reagent is a common protocol in pyrazole chemistry. An efficient microwave‐assisted synthesis of 4‐formylpyrazoles by employing Vilsmeier‐Haack reagent (OPC‐VH) derived from phthaloyl dichloride/dimethylformamide has been described. This method offers the advantages of operational simplicity, avoiding the use of POCl3 as toxic reagents and reuse of the by‐product in the preparation of phthaloyl dichloride.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jhet.3824</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8956-5558</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-152X |
ispartof | Journal of heterocyclic chemistry, 2020-02, Vol.57 (2), p.796-804 |
issn | 0022-152X 1943-5193 |
language | eng |
recordid | cdi_proquest_journals_2352033472 |
source | Wiley Online Library |
subjects | Chemical synthesis Dichlorides Organic chemistry Pyrazole Reagents |
title | Microwave‐assisted Vilsmeier‐Haack synthesis of Pyrazole‐4‐carbaldehydes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T02%3A25%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Microwave%E2%80%90assisted%20Vilsmeier%E2%80%90Haack%20synthesis%20of%20Pyrazole%E2%80%904%E2%80%90carbaldehydes&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Kumari,%20Poonam&rft.date=2020-02&rft.volume=57&rft.issue=2&rft.spage=796&rft.epage=804&rft.pages=796-804&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.3824&rft_dat=%3Cproquest_cross%3E2352033472%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2352033472&rft_id=info:pmid/&rfr_iscdi=true |