Loading…
New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones
Herein, a novel DABCO-based dicationic ionic liquid (bis-DIL) was easily prepared from the sonication of DABCO with 1,3-dichloro-2-propanol and then characterized by several techniques. Thereafter, under the ultimate green conditions, the performance of the bis-DIL was examined for the sono-synthesi...
Saved in:
Published in: | Royal Society open science 2019-07, Vol.6 (7), p.190997-190997 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3 |
container_end_page | 190997 |
container_issue | 7 |
container_start_page | 190997 |
container_title | Royal Society open science |
container_volume | 6 |
creator | Arafa, Wael A A Mourad, Asmaa K |
description | Herein, a novel DABCO-based dicationic ionic liquid (bis-DIL) was easily prepared from the sonication of DABCO with 1,3-dichloro-2-propanol and then characterized by several techniques. Thereafter, under the ultimate green conditions, the performance of the bis-DIL was examined for the sono-synthesis of a new library of bis-2-amino-5-arylidenethiazol-4-ones via one-pot pseudo-five-component Knoevenagel condensation reaction of appropriate dialdehydes, rhodanine and amines. This protocol is tolerant towards several mono- and dialdehydes, excellently high yielding and affording access to the desired products in a single step within a short reaction time. Compared with the conventional methodologies, the proposed method displayed several remarkable merits such as milder reaction conditions without any side product, green solvent media, recording well in a variety of green metrics and applicability in gram-scale production. The recyclability of the bis-DIL was also investigated with an average recovered yield of 97% for six sequential cycles without any significant loss of the activity. |
doi_str_mv | 10.1098/rsos.190997 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_ebdedd5fe568490792c0d52de43d31bc</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_ebdedd5fe568490792c0d52de43d31bc</doaj_id><sourcerecordid>2275263152</sourcerecordid><originalsourceid>FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3</originalsourceid><addsrcrecordid>eNpVkc1v1DAQxSMEolXpiTvyEQm59UdsxxyQyvJVqaIXOFsTe9J15Y23dhbU_vVkSVu1pxnNvPnNk17TvOXshDPbnZaa6wm3zFrzojkUTLVUGSZfPukPmuNarxljXDFptHndHEjecmN0d9jc_cS_JEQPU8xj9OTL2efVJe2hYiDLJMWbXQz1IwFSPSToE5INTpDoUBBJHpFu80Tq7TitscZK8kD6WKmgsIljpopCuU0x4IjTOsJdTrSl81V907waIFU8vq9Hze9vX3-tftCLy-_nq7ML6pUxE9WGia7H1huwfGhlqwT6YQClvDQBrBIKhfVGB6GEFV5pGHrGRcusUsqAPGrOF27IcO22JW5mQy5DdP8HuVw5KFP0CR32AUNQAyrdtZaZGceCEgFbGSTv_cz6tLC2u36DweM4FUjPoM83Y1y7q_zHad1ZzcQMeH8PKPlmh3Vym1g9pgQj5l11QhgltORqL_2wSH3JtRYcHt9w5vbhu334bgl_Vr976uxR-xC1_AekoavP</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2275263152</pqid></control><display><type>article</type><title>New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones</title><source>Open Access: PubMed Central</source><source>Royal Society Open Access Journals</source><creator>Arafa, Wael A A ; Mourad, Asmaa K</creator><creatorcontrib>Arafa, Wael A A ; Mourad, Asmaa K</creatorcontrib><description>Herein, a novel DABCO-based dicationic ionic liquid (bis-DIL) was easily prepared from the sonication of DABCO with 1,3-dichloro-2-propanol and then characterized by several techniques. Thereafter, under the ultimate green conditions, the performance of the bis-DIL was examined for the sono-synthesis of a new library of bis-2-amino-5-arylidenethiazol-4-ones via one-pot pseudo-five-component Knoevenagel condensation reaction of appropriate dialdehydes, rhodanine and amines. This protocol is tolerant towards several mono- and dialdehydes, excellently high yielding and affording access to the desired products in a single step within a short reaction time. Compared with the conventional methodologies, the proposed method displayed several remarkable merits such as milder reaction conditions without any side product, green solvent media, recording well in a variety of green metrics and applicability in gram-scale production. The recyclability of the bis-DIL was also investigated with an average recovered yield of 97% for six sequential cycles without any significant loss of the activity.</description><identifier>ISSN: 2054-5703</identifier><identifier>EISSN: 2054-5703</identifier><identifier>DOI: 10.1098/rsos.190997</identifier><identifier>PMID: 31417768</identifier><language>eng</language><publisher>England: The Royal Society</publisher><subject>aqueous media ; bis-2-amino-5-arylidenethiazol-4-ones ; Chemistry ; dabco functionalized ionic liquids ; knoevenagel condensation ; stereoselectivity</subject><ispartof>Royal Society open science, 2019-07, Vol.6 (7), p.190997-190997</ispartof><rights>2019 The Authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3</citedby><cites>FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3</cites><orcidid>0000-0002-9288-4143</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689602/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689602/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3322,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31417768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arafa, Wael A A</creatorcontrib><creatorcontrib>Mourad, Asmaa K</creatorcontrib><title>New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones</title><title>Royal Society open science</title><addtitle>R Soc Open Sci</addtitle><description>Herein, a novel DABCO-based dicationic ionic liquid (bis-DIL) was easily prepared from the sonication of DABCO with 1,3-dichloro-2-propanol and then characterized by several techniques. Thereafter, under the ultimate green conditions, the performance of the bis-DIL was examined for the sono-synthesis of a new library of bis-2-amino-5-arylidenethiazol-4-ones via one-pot pseudo-five-component Knoevenagel condensation reaction of appropriate dialdehydes, rhodanine and amines. This protocol is tolerant towards several mono- and dialdehydes, excellently high yielding and affording access to the desired products in a single step within a short reaction time. Compared with the conventional methodologies, the proposed method displayed several remarkable merits such as milder reaction conditions without any side product, green solvent media, recording well in a variety of green metrics and applicability in gram-scale production. The recyclability of the bis-DIL was also investigated with an average recovered yield of 97% for six sequential cycles without any significant loss of the activity.</description><subject>aqueous media</subject><subject>bis-2-amino-5-arylidenethiazol-4-ones</subject><subject>Chemistry</subject><subject>dabco functionalized ionic liquids</subject><subject>knoevenagel condensation</subject><subject>stereoselectivity</subject><issn>2054-5703</issn><issn>2054-5703</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc1v1DAQxSMEolXpiTvyEQm59UdsxxyQyvJVqaIXOFsTe9J15Y23dhbU_vVkSVu1pxnNvPnNk17TvOXshDPbnZaa6wm3zFrzojkUTLVUGSZfPukPmuNarxljXDFptHndHEjecmN0d9jc_cS_JEQPU8xj9OTL2efVJe2hYiDLJMWbXQz1IwFSPSToE5INTpDoUBBJHpFu80Tq7TitscZK8kD6WKmgsIljpopCuU0x4IjTOsJdTrSl81V907waIFU8vq9Hze9vX3-tftCLy-_nq7ML6pUxE9WGia7H1huwfGhlqwT6YQClvDQBrBIKhfVGB6GEFV5pGHrGRcusUsqAPGrOF27IcO22JW5mQy5DdP8HuVw5KFP0CR32AUNQAyrdtZaZGceCEgFbGSTv_cz6tLC2u36DweM4FUjPoM83Y1y7q_zHad1ZzcQMeH8PKPlmh3Vym1g9pgQj5l11QhgltORqL_2wSH3JtRYcHt9w5vbhu334bgl_Vr976uxR-xC1_AekoavP</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Arafa, Wael A A</creator><creator>Mourad, Asmaa K</creator><general>The Royal Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9288-4143</orcidid></search><sort><creationdate>20190701</creationdate><title>New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones</title><author>Arafa, Wael A A ; Mourad, Asmaa K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>aqueous media</topic><topic>bis-2-amino-5-arylidenethiazol-4-ones</topic><topic>Chemistry</topic><topic>dabco functionalized ionic liquids</topic><topic>knoevenagel condensation</topic><topic>stereoselectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arafa, Wael A A</creatorcontrib><creatorcontrib>Mourad, Asmaa K</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Royal Society open science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arafa, Wael A A</au><au>Mourad, Asmaa K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones</atitle><jtitle>Royal Society open science</jtitle><addtitle>R Soc Open Sci</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>6</volume><issue>7</issue><spage>190997</spage><epage>190997</epage><pages>190997-190997</pages><issn>2054-5703</issn><eissn>2054-5703</eissn><abstract>Herein, a novel DABCO-based dicationic ionic liquid (bis-DIL) was easily prepared from the sonication of DABCO with 1,3-dichloro-2-propanol and then characterized by several techniques. Thereafter, under the ultimate green conditions, the performance of the bis-DIL was examined for the sono-synthesis of a new library of bis-2-amino-5-arylidenethiazol-4-ones via one-pot pseudo-five-component Knoevenagel condensation reaction of appropriate dialdehydes, rhodanine and amines. This protocol is tolerant towards several mono- and dialdehydes, excellently high yielding and affording access to the desired products in a single step within a short reaction time. Compared with the conventional methodologies, the proposed method displayed several remarkable merits such as milder reaction conditions without any side product, green solvent media, recording well in a variety of green metrics and applicability in gram-scale production. The recyclability of the bis-DIL was also investigated with an average recovered yield of 97% for six sequential cycles without any significant loss of the activity.</abstract><cop>England</cop><pub>The Royal Society</pub><pmid>31417768</pmid><doi>10.1098/rsos.190997</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9288-4143</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2054-5703 |
ispartof | Royal Society open science, 2019-07, Vol.6 (7), p.190997-190997 |
issn | 2054-5703 2054-5703 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_ebdedd5fe568490792c0d52de43d31bc |
source | Open Access: PubMed Central; Royal Society Open Access Journals |
subjects | aqueous media bis-2-amino-5-arylidenethiazol-4-ones Chemistry dabco functionalized ionic liquids knoevenagel condensation stereoselectivity |
title | New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T03%3A11%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=New%20dicationic%20DABCO-based%20ionic%20liquids:%20a%20scalable%20metal-free%20one-pot%20synthesis%20of%20bis-2-amino-5-arylidenethiazol-4-ones&rft.jtitle=Royal%20Society%20open%20science&rft.au=Arafa,%20Wael%20A%20A&rft.date=2019-07-01&rft.volume=6&rft.issue=7&rft.spage=190997&rft.epage=190997&rft.pages=190997-190997&rft.issn=2054-5703&rft.eissn=2054-5703&rft_id=info:doi/10.1098/rsos.190997&rft_dat=%3Cproquest_doaj_%3E2275263152%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c577t-67028be4c7a91f43452ecffa55c37da9525e29c76d25292c56afb0124095557a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2275263152&rft_id=info:pmid/31417768&rfr_iscdi=true |