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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675184Generated: November 2, 2026

Diethyl Ether → Benzyl 3-benzyl-2,2-dimethyl-4-oxoimidazolidine-1-carboxylate

https://huagongshe.com/reaction/1675184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium bisulfateHCID 516920—
Reactant3-Benzyl-2,2-dimethylimidazolidin-4-oneHCID 57433089—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-benzyl-2,2-dimethyl-4-oxoimidazolidine-1-carboxylateHCID 57433090—

Reaction Steps

A cold (0° C.) solution of 3-benzyl-2,2-dimethylimidazolidin-4 -one (2.28 g, 11.16 mmol) in CH2Cl2 (25 mL) was treated with benzylchloroformate (0.96 mL, 6.70 mmol), a solution of 4-dimethylaminopyridine (1.71 g, 13.95 mmol) in CH2Cl2 (10 mL), and again with benzylchloroformate (0.96 mL, 6.70 mmol). The solution was stirred for 30 min and poured into aqueous 10% KHSO4 solution. The layers were separated, and the organic was washed twice with water and once with brine. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to afford an orange oil. The oil was treated with Et2O causing a precipitate which was filtered to afford the product as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.37 (m, 10H), 5.14 (s, 2H), 4.54 (s, 2H), 4.11 (s, 6H), 1.56 (s, 6H); ES MS (M+1)=339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003653B2
Source datasetuspto-grants-2011_08
ORD IDord-e45e0781e6024429be02e05fe2ff6c85
Source noteuspto-grants-2011_08