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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762979Generated: October 31, 2026

Hydrochloric Acid → 3-Methyl-5-(2,2,2-trifluoroethoxy)-1,2-thiazole-4-sulfonyl chloride

https://huagongshe.com/reaction/1762979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphoric AcidHCID 1004—
ReactantSulfur DioxideHCID 1119—
ReactantHCID 14328732HCID 14328732—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
Product3-Methyl-5-(2,2,2-trifluoroethoxy)-1,2-thiazole-4-sulfonyl chlorideHCID 14574917—

Reaction Conditions

Temperature-5 °C

Reaction Steps

5 ml of acetic acid, 6 ml of 85% phosphoric acid, and 3 ml of concentrated hydrochloric acid was added to 2.1 g of 4-amino-3-methyl-5-(2,2,2-trifluoroethoxy)isothiazole prepared in the above step (2). 2 ml of aqueous solution containing 0.77 g of sodium nitrite was added dropwise to the above mixture at -20° to -10° C. The resulted solution was stirred at -5° C. for 30 minutes and was gradually added dropwise at -10° to -5° C. into 30 ml of an acetic acid solution, which had been saturated with sulfur dioxide and had contained 0.3 g of cuprous chloride. After the completion of dropping, the resulted solution was stirred and reacted at 0° to 5° C. for an hour. After the completion of the reaction, the reaction mixture was poured into ice-cold water, and was extracted with dichloromethane, and the extracted layer was sufficiently washed with water and dried. The solvent was subjected to distillation under reduced pressure to give 1.2 g of oily 3-methyl-5-(2,2,2-trifluoroethoxy)-4-isothiazolesulfonyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835282
Source datasetuspto-grants-1989_05
ORD IDord-164eb255c23e42c09ebd314bf888c5c1
Source noteuspto-grants-1989_05