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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226994Generated: October 31, 2026

Water → HCID 10857002, compound

https://huagongshe.com/reaction/2226994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydantoinHCID 10006—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl chloromethyl etherHCID 137983—
CatalystEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 10857002HCID 1085700270%

Reaction Steps

In 5 ml of methyl isobutyl ketone were suspended 216 mg (3.85 mmoles) of potassium hydroxide and 73 mg (0.226 mmoles) of tris[2-(2-methoxyethoxy)ethyl]-amine followed by addition of 900 mg (8.99 mmoles) of imidazolidine-2,4-dione, and the mixture was stirred at room temperature for 10 minutes. Then, 704 mg (4.50 mmoles) of benzyloxymethyl chloride was added dropwise at 0° C. and the mixture was stirred at room temperature for 3 hours. To this reaction mixture was added water and the organic layer was separated and washed successively with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was subjected to silica gel chromatography (eluent: hexane:ethyl acetate =1:1) to give 687 mg (3.12 mmoles) of 3-benzyloxymethylimidazolidine-2,4-dione. Yield 70% (based on benzyloxymethyl chloride) 1H-NMR, δ(CDCl3): 3.90 (2H, s), 4.60 (2H, s), 5.05 (2H, s), 6.00-6.20 (1H, brs, -NH), 7.20-7.45 (5H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350859
Source datasetuspto-grants-1994_09
ORD IDord-3a0c7ad92686481eab2d1eeb84d24593
Source noteuspto-grants-1994_09