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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052216Generated: October 27, 2026

Pyridine → 2-Bromo-4-trichloroacetamidothiazole

https://huagongshe.com/reaction/2052216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantSodium AcetateHCID 517045—
Reactant2-Bromo-1,3-thiazol-4-amine--hydrogen bromide (1/1)HCID 20294041—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-trichloroacetamidothiazoleHCID 2037717353.9%

Reaction Steps

4-Amino-2-bromo-thiazole hydrobromide (15.6g) and trichloroacetyl chloride (14.3 g) were suspended in methylene chloride (100 ml) with stirring and treated dropwise with pyridine (16 ml) over 15 minutes maintaining reaction temperatures at 0° C. with an ice bath. After completing the addition, the reaction mixture was stirred at room temperature for 3 hours, then poured onto 20% aqueous sodium acetate (250 ml.) and stirred for 30 minutes. The mixture was separated and the organic layer washed with 2N hydrochloric acid, water, sodium carbonate solution and water. The organic layer was dried (MgSO4) and the solvent removed in vacuo and the residue treated with charcoal in hexane and recrystallised from hexane to give the title compound (10.5g) m.p. 77°-80° C. (Found: C, 19.0; H, 0.7 N, 8.5. C5H2Cl3BrN2OS requires C, 18.5; H, 0.6; N, 8.6%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04183854
Source datasetuspto-grants-1980_01
ORD IDord-074eb83e4db84bbcb72d3a1211866ea4
Source noteuspto-grants-1980_01