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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213523Generated: November 1, 2026

Thionyl Chloride → 2-Chloro-4-methyl-1,3-thiazole-5-sulfonyl chloride

https://huagongshe.com/reaction/2213523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantChlorosulfonic acidHCID 24638—
Reactant2-Chloro-4-methylthiazoleHCID 3015328—
Product2-Chloro-4-methyl-1,3-thiazole-5-sulfonyl chlorideHCID 1209425089.9%

Reaction Steps

At room temperature, 150 g (1.12 mol) of 2-chloro-4-methyl-1,3-thiazole are added dropwise to a solution of 331 g (2.81 mol) of thionyl chloride in 653 g (5.61 mol) of chlorosulphonic acid. The solution is heated at reflux for 48 h. The mixture is then poured into 3 l of ice-water and extracted with 4×400 ml of dichloromethane. The combined organic phases are washed with 2.5 l of water, dried over sodium sulphate and concentrated. Distillation of the crude product gives 233.7 g of product in the form of an oil. (Bp 87-96° C., 0.7 mbar, GC 98.1%, yield 89.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105553B2
Source datasetuspto-grants-2006_09
ORD IDord-a6a7872e69fe4073bac7cd573bc36774
Source noteuspto-grants-2006_09