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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329397Generated: October 29, 2026

Acetic Acid → 4-(4-(2-Chloroethyl)phenyl)thiazol-2-one

https://huagongshe.com/reaction/329397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBromineHCID 24408—
Reactant4'-(beta-Chloroethyl)acetophenoneHCID 144359—
ReactantPotassium thiocyanateHCID 516872—
SolventEthyl AcetateHCID 8857—
Product4-(4-(2-Chloroethyl)phenyl)thiazol-2-oneHCID 1505421468%

Reaction Steps

To a 125 ml round-bottomed flask equipped with N2 inlet were added 9.1 g (50 mmol) of 4-(2-chloroethyl)acetophenone and 25 ml acetic acid. To the stirred solution was added 2.58 ml (50 mmol) of bromine dropwise over 2 minutes. The reaction was stirred at room temperature for 30 minutes, taken up in ethyl acetate, washed with water, saturated aqueous sodium bicarbonate solution, and brine, dried over sodium sulfate, and evaporated to an oil. The oil was taken up in 250 ml of acetone, treated with 4.9 g (50 mmol) of potassium thiocyanate, and stirred at room temperature for 3 hours. The precipitate was filtered and the filtrate evaporated. The residue was taken up in ethyl acetate, washed with water and brine, dried over sodium sulfate, and evaporated to a solid. The solid was taken up in 100 ml of boiling ethanol and treated slowly with 83 ml of 1N HCl, then refluxed for 14 hours. The reaction was cooled and the precipitate filtered, washed with water, and dried to give 8.2 g (68%) of a white solid, m.p. 226°-229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891375
Source datasetuspto-grants-1990_01
ORD IDord-cc970eb3794b42dfbd6d7eb504dda213
Source noteuspto-grants-1990_01