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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443774Generated: October 29, 2026

Water → N-(1,3-thiazol-2-yl)-4-nitro-2-trichloromethylphenylsulfenamide

https://huagongshe.com/reaction/443774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-AminothiazoleHCID 2155—
Reactant4-Nitro-2-trichloromethylbenzenesulfenyl chlorideHCID 12763555—
SolventTetrahydrofuranHCID 8028—
ProductN-(1,3-thiazol-2-yl)-4-nitro-2-trichloromethylphenylsulfenamideHCID 2346539870%

Reaction Conditions

Temperature10 °C

Reaction Steps

40 g of 2-aminothiazole is dissolved in 500 ml of tetrahydrofuran; while stirring and at 10° C., 61.4 g of 4-nitro-2-trichloromethylbenzenesulfenyl chloride is added. The addition of water precipitates the sulfenamide, which is filtered and recrystallized from ethyl acetate. There is obtained 50 g (70% of theory) of N-(1,3-thiazol-2-yl)-4-nitro-2-trichloromethylphenylsulfenamide; m.p.: 165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261924
Source datasetuspto-grants-1981_04
ORD IDord-8639666210024c48959d2c2918f0497a
Source noteuspto-grants-1981_04