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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816178Generated: October 31, 2026

p-Chlorophenacyl bromide → HCID 22496401, compound

https://huagongshe.com/reaction/1816178

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[4-(Trifluoromethyl)phenyl]thioureaHCID 2777727—
SolventEthanolHCID 702—
ProductHCID 22496401HCID 2249640193%

Reaction Steps

(4-Trifluoromethylphenyl)thiourea (5.00 g; 22.7 mmol) was dissolved in ethanol (45 mL) by gentle heating. Then, α-bromo-p-chloroacetophenone (5.30 g; 22.70 mmol) and DIPEA (3.22 g; 24.9 mmol) was added. The resulting solution was stirred for 16 hours at ambient temperature. The mixture was then concentrated in vacuo, and the residue dissolved in ethyl acetate. The DIPEA hydrobromide, which crystallized out of solution, was removed by filtration. The filtrate was washed with water (2×50 mL) and brine (50 mL), and dried over anhydrous sodium sulphate. The solvent was removed by rotary evaporation to give 7.00 g (93%) of [4-(4-chlorophenyl)thiazol-2-yl]-(4-trifluoromethylphenyl)amine as an oil. The material was pure enough for use in the next step (a crystalline sample can be obtained by re-crystallization in heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881746B2
Source datasetuspto-grants-2005_04
ORD IDord-59ebc67e009047728677944530ebbf39
Source noteuspto-grants-2005_04