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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483976Generated: October 27, 2026

2-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-one → 2-Acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazole

https://huagongshe.com/reaction/483976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-oneHCID 3862523—
ReactantN-(2-amino-2-thioxoethyl)acetamideHCID 4435531—
SolventEthanolHCID 702—
Product2-Acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazoleHCID 1004454033.2%

Reaction Steps

A mixture of 1,2-bis(4-methoxyphenyl)-2-chloroethanone (5.99 g) and 2-(acetylamino)ethanethioamide (3.00 g) in ethanol (30 ml) was refluxed for 2 hours. After allowing to cool to room temperature, the solvent was evaporated in vacuo, and the residue was dissolved in chloroform (200 ml) and aqueous solution of sodium hydrogencarbonate (200 ml). The separated organic layer was washed with water and brine, dried over magnesium sulfate and treated with activated charcoal. After filtration, the filtrate was evaporated in vacuo. The resulting residue was dissolved in diethyl ether, added ethanol solution of hydrogen chloride, and the resulting precipitate was collected by filtration. The resulting crude compound was recrystallized with ethanol (10 ml). And the resulting crystal was collected by filtration, washed with ethanol and diethyl ether, and dried to give 2-acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazole (2.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229386
Source datasetuspto-grants-1993_07
ORD IDord-1dadf65eb7cf4d2b92495264e5d079a6
Source noteuspto-grants-1993_07