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A Practical Access to Functionalized Alkyl Sulfinates

Authors :
Benjamin Flamme
Mansour Haddad
Christine Tran
Alexandre Chagnes
Phannarath Phansavath
Virginie Ratovelomanana-Vidal
Université Paris sciences et lettres (PSL)
GeoRessources
Centre National de la Recherche Scientifique (CNRS)-Université de Lorraine (UL)-Centre de recherches sur la géologie des matières premières minérales et énergétiques (CREGU)-Institut national des sciences de l'Univers (INSU - CNRS)
Source :
SYNLETT, SYNLETT, Georg Thieme Verlag, 2018, 29 (12), pp.1622-1626. ⟨10.1055/s-0036-1591588⟩
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

International audience; Sulfinates, basic forms of sulfinic acids, constitute key intermediates in organic synthesis for their stability. Given the limited commercial availability of the aliphatic derivatives and the several drawbacks regarding their synthesis, the preparation of alkyl sulfinates remains a challenge. Within the frame of the development of approaches for the conception of aliphatic sulfinates, we describe herein a three-step synthesis of aliphatic sulfinates. This cost-effective method involves the use of 2-mercaptobenzothiazole under mild conditions and exhibits good yields (up to 78% over three steps). This approach provides an access to a wide range of functionalized sulfinates. A good tolerance with respect to diverse functional groups (alkene, alkyne, ether, acetal) was also noted.

Details

Language :
English
ISSN :
09365214 and 14372096
Database :
OpenAIRE
Journal :
SYNLETT, SYNLETT, Georg Thieme Verlag, 2018, 29 (12), pp.1622-1626. ⟨10.1055/s-0036-1591588⟩
Accession number :
edsair.doi.dedup.....b744bb0de0d5f5db66e488f26071ba6f
Full Text :
https://doi.org/10.1055/s-0036-1591588⟩