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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881688Generated: November 3, 2026

Pyridine → 3-(Trifluoromethyl)benzenesulfonyl chloride

https://huagongshe.com/reaction/1881688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
Reactant2-Chloro-6-methylbenzene-1-sulfonyl chlorideHCID 15725370—
SolventWaterHCID 962—
Product3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—

Reaction Steps

2-Chloro-6-methylbenzenesulfonyl chloride (8, 7.82 g, 34.8 mmol) was added to a solution of 7 (8.83 g, 31.6 mmol) in pyridine (7.67 ml, 95.0 mmol) and the reaction mixture was stirred at room temperature overnight. CH2Cl2 and H2O were added to the reaction mixture and the organic phase was separated, washed with water and sat. NaCl solution, dried over Na2SO4 and concentrated to obtain the product 9, which was employed directly as such in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318769B2
Source datasetuspto-grants-2012_11
ORD IDord-95cbadb8c3bb41a2be08fd8d9b9cf1ad
Source noteuspto-grants-2012_11