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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107682Generated: October 30, 2026

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

https://huagongshe.com/reaction/1107682

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 numberUS06063734
Source datasetuspto-grants-2000_05
ORD IDord-fa5f84e32bd74bcbaa1ce2493f116548
Source noteuspto-grants-2000_05