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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465890Generated: October 31, 2026

Lawesson's reagent → 4-Chloro-3,5-bis(trifluoromethyl)benzothioamide

https://huagongshe.com/reaction/1465890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant4-Chloro-3,5-bis(trifluoromethyl)benzamideHCID 86730370—
SolventTolueneHCID 1140—
Product4-Chloro-3,5-bis(trifluoromethyl)benzothioamideHCID 8673036979%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-chloro-3,5-bis(trifluoromethyl)benzamide (1.2 g) in toluene (20 mL) was added Lawesson's reagent (3.32 g, 2.0 eq.). The reaction mixture was stirred at 90° C. for 8 h before being cooled to room temperature and filtered. The filtrate was poured into water and extracted with EtOAc (3×100 mL). The combined organic extracts were washed with brine (3×50 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure (25° C., 20 mmHg) to afford 2 g of crude compound. The crude compound was purified by combi-flash chromatography (eluting with 7% EtOAc:hexane) to afford 1.0 g of desired compound (yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999996B2
Source datasetuspto-grants-2015_04
ORD IDord-a33a81295bdf4112ab6861443d748f3d
Source noteuspto-grants-2015_04