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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717632Generated: October 30, 2026

2-Imidazolidinone → HCID 68700715, compound

https://huagongshe.com/reaction/717632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ImidazolidinoneHCID 8453—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
ProductHCID 68700715HCID 6870071526.1%

Reaction Steps

To a solution of imidazolidin-2-one (0.2 g; 2.3 mmol) in anhydrous DMF (5 ml) 60% NaH in mineral oil (0.18 g; 4.6 mmol) was added at room temperature, under N2. After stirring for 1 h, tert-butyl 2-bromoacetate (0.35 ml; 2.3 mmol) was added. The resulting mixture was stirred for additional 2 h and solvents were removed in vacuo. The residue was diluted to 15 ml with EtOAc, washed with H2O, brine, dried over anhydrous MgSO4 and filtered. The filtrate was evaporated under reduced pressure and the residue was purified by FCC (SiO2, EtOAc) to give the title compound (0.12 g; 26%) as a colourless solid. 1H-NMR (CDCl3) 4.61 (broad s, 1H); 3.83 (s, 2H); 3.58-3.41 (m, 4H); 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193716B2
Source datasetuspto-grants-2015_11
ORD IDord-96b9bfa6f8874a1e88342efcc4541ef6
Source noteuspto-grants-2015_11