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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350709Generated: October 26, 2026

Ethanol → Thiazole, 4-(4-chlorophenyl)-5-methyl-2-phenyl-

https://huagongshe.com/reaction/350709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium AcetateHCID 517045—
ReactantThiobenzamideHCID 683563—
Reactant2-Bromo-1-(4-chlorophenyl)propan-1-oneHCID 3788219—
SolventWaterHCID 962—
ProductThiazole, 4-(4-chlorophenyl)-5-methyl-2-phenyl-HCID 803641468.2%

Reaction Steps

A mixture of 2-bromo-4′-chloropropiophenone (45.0 g), thiobenzamide (24.7 g), sodium acetate (14.8 g) and ethanol (400 mL) was stirred with heating under reflux for 3 hrs. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated to give 4-(4-chlorophenyl)-5-methyl-2-phenylthiazole (35.1 g, 68%) as crystals. Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 90–91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183276B2
Source datasetuspto-grants-2007_02
ORD IDord-e8f752d4746b4f299475521265f288a2
Source noteuspto-grants-2007_02