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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916464Generated: October 27, 2026

Hydantoin → 3-(3-Benzyloxypropyl)imidazolidine-2,4-dione

https://huagongshe.com/reaction/916464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydantoinHCID 10006—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant3-Benzyloxy-1-propanolHCID 347971—
SolventDichloromethaneHCID 6344—
Product3-(3-Benzyloxypropyl)imidazolidine-2,4-dioneHCID 6701922653%

Reaction Conditions

Temperature0 °C

Reaction Steps

Imidazolidine-2,4-dione (1.0 g, 9.99 mmol), 3-benzyloxypropan-1-ol (1.9 ml, 12.0 mmol) and triphenylphosphine (3.1 g, 12.0 mmol) were stirred in methylene chloride (20 ml) and cooled to 0° C. Diisopropyl azodicarboxylate (2.36 μl, 12.0 mmol) in dichloromethane (5 ml) was slowly added and the mixture stirred at ambient temperature overnight. The mixture was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by column chromatography eluting with methylene chloride/methanol (98/2) to give 3-(3-benzyloxypropyl)imidazolidine-2,4-dione (1.3 g, 53%, containing 7% w/w triphenylphosphine oxide) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268230B2
Source datasetuspto-grants-2007_09
ORD IDord-5d04e0b461664f33a1fb7f32f9e00ff0
Source noteuspto-grants-2007_09