New Protocol for the Synthesis of S-Thioesters from Benzylic, Allylic and Tertiary Alcohols with Thioacetic Acid.

Autor: Lachguar A; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France.; IUT A Paul Sabatier, Dpt. De Chimie, Ave. G. Pompidou, 81104, Castres Cedex, France., Bandyopadhyay U; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France., Ech-Chariy M; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France.; IUT A Paul Sabatier, Dpt. De Chimie, Ave. G. Pompidou, 81104, Castres Cedex, France., Vincendeau S; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France., Audin C; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France.; IUT A Paul Sabatier, Dpt. De Chimie, Ave. G. Pompidou, 81104, Castres Cedex, France., Daran JC; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France., Manoury E; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France., Poli R; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France.; Institut Universitaire de France, 1, rue Descartes, 75231, Paris, France., Deydier E; LCC-CNRS, Université de Toulouse, UPS, INPT, 205 Route de Narbonne, 31077, Toulouse, Cedex 4, France.; IUT A Paul Sabatier, Dpt. De Chimie, Ave. G. Pompidou, 81104, Castres Cedex, France.
Jazyk: angličtina
Zdroj: Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2024 Jan 02; Vol. 30 (1), pp. e202302551. Date of Electronic Publication: 2023 Nov 13.
DOI: 10.1002/chem.202302551
Abstrakt: A new one-pot solvent-less reaction to convert benzylic, allylic, ferrocenyl or tertiary alcohols into S-thioesters, bench-stable and less odorous precursors of the corresponding thiols, which is based on reactions in neat thioacetic acid in the presence of tetrafluoroboric acid, is presented. Reaction monitoring by NMR and GC of the benzyl alcohol conversion indicated the intermediate formation of benzyl acetate and benzyl thionoacetate (PhCH 2 OC(S)CH 3 ) prior to the slower conversion to the final S-benzyl thioacetate product. Increasing the HBF 4 concentration enhanced the reaction rate, giving good to excellent yield (up to 99 %) for a large scope of alcohols. Control experiments, with support of DFT calculations, have revealed a thermodynamically favorable, though requiring HBF 4 -activation, disproportionation of CH 3 C(O)SH to CH 3 C(O)OH and CH 3 C(S)SH, the latter immediately decomposing to H 2 S and (MeC) 4 S 6 but also generating the hitherto unreported [MeC(O)C(Me)S] 2 (μ-S) 2 . Kinetic investigations demonstrated that the rate of benzyl alcohol conversion is second-order in [PhCH 2 OH] and second order in [HBF 4 ], while the rate of conversion of the benzyl acetate intermediate to S-benzyl thioacetate is second order in [PhCOOMe] and fourth order in [HBF 4 ]. The DFT calculations rationalize the need to two alcohol molecules and two protons to generate the reactive benzyl cation.
(© 2023 Wiley-VCH GmbH.)
Databáze: MEDLINE
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