Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides

An improved and efficient method for the synthesis of thioamides is presented. For this transformation, dimethylamine as the key intermediate is generated in situ from dimethylformamide (DMF). All the tested substrates produced the desired products with excellent isolated yields.

Bibliographic Details
Main Authors: Weibing Liu, Cui Chen, Hailing Liu
Format: Article
Language:English
Published: Beilstein-Institut 2015-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.11.187
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author Weibing Liu
Cui Chen
Hailing Liu
author_facet Weibing Liu
Cui Chen
Hailing Liu
author_sort Weibing Liu
collection DOAJ
description An improved and efficient method for the synthesis of thioamides is presented. For this transformation, dimethylamine as the key intermediate is generated in situ from dimethylformamide (DMF). All the tested substrates produced the desired products with excellent isolated yields.
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spelling doaj.art-d48be1423c7e4d849f5bd8e5950633802022-12-21T22:11:48ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972015-09-011111721172610.3762/bjoc.11.1871860-5397-11-187Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamidesWeibing Liu0Cui Chen1Hailing Liu2College of Chemical Engineering, Guangdong University of Petrochemical Technology, 2 Guandu Road, Maoming 525000, P. R. China, Fax: +86-668-2923575; Tel: +86-668-2923956College of Chemical Engineering, Guangdong University of Petrochemical Technology, 2 Guandu Road, Maoming 525000, P. R. China, Fax: +86-668-2923575; Tel: +86-668-2923956College Analytical and Testing Centre, Beijing Normal University, No. 19, Xinjiekouwai St., Haidian District, Beijing 100875, P. R. China; Tel: +86-15010928428An improved and efficient method for the synthesis of thioamides is presented. For this transformation, dimethylamine as the key intermediate is generated in situ from dimethylformamide (DMF). All the tested substrates produced the desired products with excellent isolated yields.https://doi.org/10.3762/bjoc.11.187aldehydesdimethylformamide (DMF)elemental sulfurketonesthioamides
spellingShingle Weibing Liu
Cui Chen
Hailing Liu
Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
Beilstein Journal of Organic Chemistry
aldehydes
dimethylformamide (DMF)
elemental sulfur
ketones
thioamides
title Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
title_full Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
title_fullStr Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
title_full_unstemmed Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
title_short Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
title_sort dimethylamine as the key intermediate generated in situ from dimethylformamide dmf for the synthesis of thioamides
topic aldehydes
dimethylformamide (DMF)
elemental sulfur
ketones
thioamides
url https://doi.org/10.3762/bjoc.11.187
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AT cuichen dimethylamineasthekeyintermediategeneratedinsitufromdimethylformamidedmfforthesynthesisofthioamides
AT hailingliu dimethylamineasthekeyintermediategeneratedinsitufromdimethylformamidedmfforthesynthesisofthioamides