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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980295Generated: October 26, 2026

(4S)-3-Benzyloxycarbonyl-1-methyl-2-oxoimidazolidine-4-carboxylic acid tert-butyl ester → tert-Butyl (4S)-1-methyl-2-oxoimidazolidine-4-carboxylate

https://huagongshe.com/reaction/1980295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4S)-3-Benzyloxycarbonyl-1-methyl-2-oxoimidazolidine-4-carboxylic acid tert-butyl esterHCID 13053974—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
Producttert-Butyl (4S)-1-methyl-2-oxoimidazolidine-4-carboxylateHCID 1305397698.2%

Reaction Steps

8.5 g of tert.-butyl (4S)-1-methyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are dissolved in 200 ml of methanol, and 0.1 g of palladium black is added thereto. The mixture is shaken at room temperature in hydrogen gas atmosphere under atmospheric pressure. After the reaction the catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue obtained is washed with n-hexane. 5.0 g of tert.-butyl (4S)-1-methyl-2-oxo-imidazolidine-4-carboxylate are obtained as colorless crystals. Yield: 98.2%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508727
Source datasetuspto-grants-1985_04
ORD IDord-2a99e26b85cc4317a8256e0be7222d00
Source noteuspto-grants-1985_04