Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors

Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up. The reaction product on a >100 gram scale can...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2020-04, Vol.22 (8), p.2399-242
Hauptverfasser: Pedersen, Martin Jæger, Jurys, Arminas, Pedersen, Christian Marcus
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 242
container_issue 8
container_start_page 2399
container_title Green chemistry : an international journal and green chemistry resource : GC
container_volume 22
creator Pedersen, Martin Jæger
Jurys, Arminas
Pedersen, Christian Marcus
description Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up. The reaction product on a >100 gram scale can be purified by a single purification method, such as distillation or precipitation. The overall yield is above 50%. Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone.
doi_str_mv 10.1039/d0gc00770f
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2394903048</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2394903048</sourcerecordid><originalsourceid>FETCH-LOGICAL-c303t-a3ef6292e44883119bebddc39edf80b853a5cbf3bf3411c5e3c1cdbef6c14ab93</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMoWKsX70LEm7iabLIfOUprq1DwoJ6XZJLYrdvumtkF99-7tlJvwsAMzPPOwEPIOWe3nAl1Z9k7MJZlzB-QEZepiFScscP9nMbH5ARxxRjnWSpHBF5AV9pUjmK_aZcOS6S1p8vehvqrX7t22VdUVx995bugN7VuHVKNFNttKL5Jou3ClqCDGSJVCVRDaWkTHHQB64Cn5MjrCt3Zbx-Tt9nD6-QxWjzPnyb3iwgEE22khfNprGInZZ4LzpVxxloQylmfM5MnQidgvBhKcg6JE8DBmiEEXGqjxJhc7e42of7sHLbFqu7CZnhZxEJJxQST-UBd7ygINWJwvmhCudahLzgrfiQWUzafbCXOBvhyBweEPfcnuWisH5iL_xjxDaQifFw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2394903048</pqid></control><display><type>article</type><title>Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Pedersen, Martin Jæger ; Jurys, Arminas ; Pedersen, Christian Marcus</creator><creatorcontrib>Pedersen, Martin Jæger ; Jurys, Arminas ; Pedersen, Christian Marcus</creatorcontrib><description>Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up. The reaction product on a &gt;100 gram scale can be purified by a single purification method, such as distillation or precipitation. The overall yield is above 50%. Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/d0gc00770f</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Distillation ; Gluconolactone ; Green chemistry ; Purification ; Reaction products ; Reagents</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2020-04, Vol.22 (8), p.2399-242</ispartof><rights>Copyright Royal Society of Chemistry 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c303t-a3ef6292e44883119bebddc39edf80b853a5cbf3bf3411c5e3c1cdbef6c14ab93</cites><orcidid>0000-0003-3223-3661 ; 0000-0003-4661-4895</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Pedersen, Martin Jæger</creatorcontrib><creatorcontrib>Jurys, Arminas</creatorcontrib><creatorcontrib>Pedersen, Christian Marcus</creatorcontrib><title>Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up. The reaction product on a &gt;100 gram scale can be purified by a single purification method, such as distillation or precipitation. The overall yield is above 50%. Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone.</description><subject>Distillation</subject><subject>Gluconolactone</subject><subject>Green chemistry</subject><subject>Purification</subject><subject>Reaction products</subject><subject>Reagents</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWKsX70LEm7iabLIfOUprq1DwoJ6XZJLYrdvumtkF99-7tlJvwsAMzPPOwEPIOWe3nAl1Z9k7MJZlzB-QEZepiFScscP9nMbH5ARxxRjnWSpHBF5AV9pUjmK_aZcOS6S1p8vehvqrX7t22VdUVx995bugN7VuHVKNFNttKL5Jou3ClqCDGSJVCVRDaWkTHHQB64Cn5MjrCt3Zbx-Tt9nD6-QxWjzPnyb3iwgEE22khfNprGInZZ4LzpVxxloQylmfM5MnQidgvBhKcg6JE8DBmiEEXGqjxJhc7e42of7sHLbFqu7CZnhZxEJJxQST-UBd7ygINWJwvmhCudahLzgrfiQWUzafbCXOBvhyBweEPfcnuWisH5iL_xjxDaQifFw</recordid><startdate>20200427</startdate><enddate>20200427</enddate><creator>Pedersen, Martin Jæger</creator><creator>Jurys, Arminas</creator><creator>Pedersen, Christian Marcus</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U6</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0003-3223-3661</orcidid><orcidid>https://orcid.org/0000-0003-4661-4895</orcidid></search><sort><creationdate>20200427</creationdate><title>Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors</title><author>Pedersen, Martin Jæger ; Jurys, Arminas ; Pedersen, Christian Marcus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-a3ef6292e44883119bebddc39edf80b853a5cbf3bf3411c5e3c1cdbef6c14ab93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Distillation</topic><topic>Gluconolactone</topic><topic>Green chemistry</topic><topic>Purification</topic><topic>Reaction products</topic><topic>Reagents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pedersen, Martin Jæger</creatorcontrib><creatorcontrib>Jurys, Arminas</creatorcontrib><creatorcontrib>Pedersen, Christian Marcus</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pedersen, Martin Jæger</au><au>Jurys, Arminas</au><au>Pedersen, Christian Marcus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2020-04-27</date><risdate>2020</risdate><volume>22</volume><issue>8</issue><spage>2399</spage><epage>242</epage><pages>2399-242</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up. The reaction product on a &gt;100 gram scale can be purified by a single purification method, such as distillation or precipitation. The overall yield is above 50%. Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d0gc00770f</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-3223-3661</orcidid><orcidid>https://orcid.org/0000-0003-4661-4895</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1463-9262
ispartof Green chemistry : an international journal and green chemistry resource : GC, 2020-04, Vol.22 (8), p.2399-242
issn 1463-9262
1463-9270
language eng
recordid cdi_proquest_journals_2394903048
source Royal Society Of Chemistry Journals; Alma/SFX Local Collection
subjects Distillation
Gluconolactone
Green chemistry
Purification
Reaction products
Reagents
title Scalable synthesis of hydroxymethyl alkylfuranoates as stable 2,5-furandicarboxylic acid precursors
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T14%3A46%3A25IST&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=Scalable%20synthesis%20of%20hydroxymethyl%20alkylfuranoates%20as%20stable%202,5-furandicarboxylic%20acid%20precursors&rft.jtitle=Green%20chemistry%20:%20an%20international%20journal%20and%20green%20chemistry%20resource%20:%20GC&rft.au=Pedersen,%20Martin%20J%C3%A6ger&rft.date=2020-04-27&rft.volume=22&rft.issue=8&rft.spage=2399&rft.epage=242&rft.pages=2399-242&rft.issn=1463-9262&rft.eissn=1463-9270&rft_id=info:doi/10.1039/d0gc00770f&rft_dat=%3Cproquest_cross%3E2394903048%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=2394903048&rft_id=info:pmid/&rfr_iscdi=true