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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822629Generated: November 2, 2026

1,3-Dichloroacetone → 4-(Chloromethyl)-2-phenyl-1,3-thiazole

https://huagongshe.com/reaction/1822629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantThiobenzamideHCID 683563—
SolventMethanolHCID 887—
Product4-(Chloromethyl)-2-phenyl-1,3-thiazoleHCID 23696957%

Reaction Steps

2.33 g of thiobenzamide was dissolved in 20 ml of dry methanol, and 2.16 g of 1,3-dichloroacetone was added thereto at room temperature and then heated under reflux for 1 hour. The solvent was distilled off under reduced pressure, and ice water was added to the remaining product, which was then neutralized with an aqueous solution of sodium hydrogen carbonate. The resulting product was extracted with ethyl acetate, washed with saturated saline, and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residual product was purified through silica gel column chromatography to obtain 2.03 g of 4-chloromethyl-2-phenylthiazole, was obtained from the fraction eluted with chloroform/n-hexane=1/2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037880B2
Source datasetuspto-grants-2006_05
ORD IDord-f8f053d60a9f4ceba200e2ceb45b3550
Source noteuspto-grants-2006_05