Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980296Generated: October 30, 2026

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

https://huagongshe.com/reaction/1980296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-benzyl 5-tert-butyl (5S)-2-oxoimidazolidine-1,5-dicarboxylateHCID 11067160—
SolventAcetoneHCID 180—
Product(4S)-3-Benzyloxycarbonyl-1-methyl-2-oxoimidazolidine-4-carboxylic acid tert-butyl esterHCID 1305397489.8%

Reaction Steps

9.6 g of tert.-butyl (4S)-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are dissolved in 200 ml of acetone, and 8.3 g of anhydrous potassium carbonate and 14.2 g of methyl iodide are added thereto. The mixture is stirred at room temperature for 6 days. The reaction mixture is treated in the same manner as described in Preparation 1-(2), whereby 9.0 g of tert.-butyl (4S)-1-methyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are obtained as colorless crystals. Yield: 89.8% The physico-chemical properties of this product are identical with those of the sample obtained in Preparation 1-(2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508727
Source datasetuspto-grants-1985_04
ORD IDord-cc448798c0ae4d1aaeb70df8e393f9d4
Source noteuspto-grants-1985_04