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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504722Generated: October 27, 2026

Acetic Acid → 2-Thiazolesulfonyl chloride

https://huagongshe.com/reaction/504722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantChlorineHCID 24526—
ReactantSodium chloride; waterHCID 57417360—
ReactantHCID 178527881HCID 178527881—
SolventDiethyl EtherHCID 3283—
Product2-Thiazolesulfonyl chlorideHCID 1157923584%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1,3-thiazole-2-thiol (5.0 g), acetic acid (150 mL) and water (50 mL) was cooled to 0° C., and chlorine gas was blown into the reaction mixture at less than 20° C. When the reaction temperature ceased to rise, blowing of the chlorine gas was stopped, and nitrogen gas was blown thereinto. The reaction mixture was diluted with diethyl ether (100 mL) and saturated brine (100 mL). The organic layer was washed successively with 10% aqueous sodium sulfite solution (100 mL), aqueous sodium hydrogencarbonate (300 mL) and saturated brine (300 mL), dried over sodium sulfate, and filtrated, the filtrate was concentrated to give the title compound (6.61 g, yield 84%) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-76b91a31d0904539b556b5c1c16ba7b2
Source noteuspto-grants-2010_08