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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34909Generated: October 27, 2026

p-Anisoyl chloride → 3-(4-Methoxybenzoyl)-4-oxothiazolidine

https://huagongshe.com/reaction/34909

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant4-ThiazolidinoneHCID 637591—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Methoxybenzoyl)-4-oxothiazolidineHCID 1385398662.9%

Reaction Steps

A solution of 4-methoxybenzoyl chloride (20.7 g) in tetrahydrofuran (50 ml) was added dropwise to a mixture of 4-oxo-thiazolidine (12.5 g) and triethylamine (16.9 ml) in tetrahydrofuran (200 ml) at -5° C. with stirring. The mixture was stirred at that temperature for 3 hours and at room temperature for 4 hours, and allowed to stand overnight. After the solvent was evaporated in vacuo, the residue was mixed with water and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate and then with water, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of ethyl acetate and n-hexane to give 3-(4-methoxybenzoyl)-4-oxothiazolidine (18.1 g) as slightly brown prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764514
Source datasetuspto-grants-1988_08
ORD IDord-2ff8a32f1b9e40a49bf580642295e58a
Source noteuspto-grants-1988_08