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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742890Generated: October 31, 2026

4-(Trifluoromethyl)benzamide → 4-(Trifluoromethyl)thiobenzamide

https://huagongshe.com/reaction/1742890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzamideHCID 74684—
ReactantLawesson's reagentHCID 87949—
SolventTolueneHCID 1140—
Product4-(Trifluoromethyl)thiobenzamideHCID 2734823—

Reaction Steps

A mixture of 4-trifluoromethylbenzamide (79 mM) and Lawesson's reagent (39 mM) in toluene (200 mL) was heated at reflux for 4 hours under N2. The reaction mixture was cooled and the resulting precipitate was isolated by filtration to give 4-trifluoromethylthiobenzamide as a solid: mp 125° C. (The following general procedure was used to synthesize the various substituted thiobenzamides (Tetrahedron 35,2433, (1979)):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05342851
Source datasetuspto-grants-1994_08
ORD IDord-492d5f40d4ba43ef87ff13b54b9e01ed
Source noteuspto-grants-1994_08