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Merck

Copper-mediated trifluoromethylthiolation of α-diazoesters.

Organic letters (2014-03-26)
Mingyou Hu, Jian Rong, Wenjun Miao, Chuanfa Ni, Yongxin Han, Jinbo Hu
초록

A novel Cu-mediated trifluoromethylthiolation of diazo compounds has been developed that provides a convenient synthetic route for the efficient α-trifluoromethylthiolation of simple esters under mild reaction conditions. The reaction is typically carried out at room temperature, and water could be used to promote the reaction.

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Sigma-Aldrich
N,N-Dimethylacetamide, ReagentPlus®, ≥99%
Sigma-Aldrich
N,N-Dimethylacetamide, suitable for peptide synthesis, ≥99.8% (GC)
Supelco
N,N-Dimethylacetamide, analytical standard
Sigma-Aldrich
N,N-Dimethylacetamide, anhydrous, 99.8%
Sigma-Aldrich
N,N-Dimethylacetamide, suitable for HPLC, ≥99.9%
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N,N-Dimethylacetamide, puriss. p.a., ≥99.5% (GC)
Sigma-Aldrich
N,N-Dimethylacetamide, ReagentPlus®, 99%
Sigma-Aldrich
N,N-Dimethylacetamide, spectrophotometric grade, ≥99%
USP
Residual Solvent Class 2 - N,N-Dimethylacetamide, United States Pharmacopeia (USP) Reference Standard