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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403398Generated: October 29, 2026

Thionyl Chloride → 3-(Methylsulfonyl)-5-(trifluoromethyl)benzoyl chloride

https://huagongshe.com/reaction/403398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 71766083HCID 71766083—
CatalystDimethylformamideHCID 6228—
Product3-(Methylsulfonyl)-5-(trifluoromethyl)benzoyl chlorideHCID 86670808102.9%

Reaction Steps

To 3-(methylsulfonyl)-5-(trifluoromethyl)benzoic acid (1 g, 3.73 mmol, example 1, intermediate d) was added N,N-dimethylformamide (27.3 mg, 28.9 μL, 373 μmol) and thionyl chloride (8.87 g, 5.44 ml, 74.5 mmol) and the suspension was heated to reflux for 30 min. A light brown solution was formed. To remove thionyl chloride, the light brown solid was diluted with toluene, followed by complete evaporation. This procedure was repeated two times to provide the desired compound as a colorless solid (1.1 g; 99%) which was pure enough for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748434B2
Source datasetuspto-grants-2014_06
ORD IDord-14b60bfe2f4b41238fc2159eb0034bb1
Source noteuspto-grants-2014_06