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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980294Generated: October 30, 2026

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

https://huagongshe.com/reaction/1980294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-benzyl 5-tert-butyl (5S)-2-oxoimidazolidine-1,5-dicarboxylateHCID 11067160—
CatalystSilver(II) oxideHCID 92152—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(4S)-3-Benzyloxycarbonyl-1-methyl-2-oxoimidazolidine-4-carboxylic acid tert-butyl esterHCID 1305397484.3%

Reaction Steps

9.6 g of tert.-butyl (4S)-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are dissolved in 200 ml of dimethylformamide, and 14.0 g of silver oxide are added thereto. 42.6 g of methyl iodide are added to the mixture at room temperature under stirring, and the mixture is further stirred for 2 days in the dark. The reaction mixture is filtered to remove insoluble materials, and the filtrate is concentrated under reduced pressure. The residue obtained is dissolved in ethyl acetate. Then, the ethyl acetate solution is washed with water, dried and concentrated under reduced pressure. The residue thus obtained is washed with n-hexane. 8.45 g of tert.-butyl (4S)-1-methyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are thereby obtained as colorless crystals. Yield: 84.3%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508727
Source datasetuspto-grants-1985_04
ORD IDord-75d9220cb3a94842a5a28097d4458f86
Source noteuspto-grants-1985_04