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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 3-Benzyl-2,2-dimethylimidazolidin-4-one | HCID 57433089 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-benzyl-2,2-dimethyl-4-oxoimidazolidine-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003653B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-e45e0781e6024429be02e05fe2ff6c85 |
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| Source note | uspto-grants-2011_08 |
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