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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292328Generated: October 31, 2026

Triethylamine → 3-[3,4-Bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide

https://huagongshe.com/reaction/2292328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Chlorocarbonyl)-1,2-phenylene diacetateHCID 14096948—
Reactant3-Amino-2-oxo-1-imidazolidinecarboxamide, monohydrochlorideHCID 131715832—
SolventDichloromethaneHCID 6344—
Product3-[3,4-Bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamideHCID 14390896314.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Amino-2-oxo-1-imidazolidinecarboxamide, monohydrochloride (12 g 0.006 mol) was suspended in 300 ml of dichloromethane. The suspension was cooled to 0° C. and 29.2 ml of triethylamine (0.198 mol) was added; the mixture was stirred for another 20 minutes. [3,4-Bis(acetyloxy)benzoyl]chloride (10.5 g) dissolved in 200 ml of dichloromethane was added dropwise with stirring at 0° C. and the mixture was stirred overnight at room temperature, filtered and treated with 50 ml of water. After stirring for 5 minutes, 3-[3,4-bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide crystallized out (7.2 g) contaminated with some triethylamine hydrochloride. The impurity was removed by treatment with water to yield 6.6 g of 3-[3,4-bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide, melting point 222°-224° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-1eb977fc06264829a978e9537a5daabf
Source noteuspto-grants-1989_01