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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702199Generated: 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/1702199

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 condensed 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% M.p. 135°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380644
Source datasetuspto-grants-1983_04
ORD IDord-1759ec4a59774265980c3c4c243f74b5
Source noteuspto-grants-1983_04