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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702204Generated: October 30, 2026

Iodoethane → tert.-butyl (4S)-1-ethyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate

https://huagongshe.com/reaction/1702204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant1-benzyl 5-tert-butyl (5S)-2-oxoimidazolidine-1,5-dicarboxylateHCID 11067160—
CatalystSilver(II) oxideHCID 92152—
SolventDimethylformamideHCID 6228—
Producttert.-butyl (4S)-1-ethyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylateHCID 1305397959.4%

Reaction Steps

9.6 g of tert.-butyl (4S)-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate, 14.0 g of silver oxide, 46.8 g of ethyl iodide and 200 ml of dimethylformamide are treated in the same manner as described in Example 1-(2). 6.2 g of tert.-butyl (4S)-1-ethyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380644
Source datasetuspto-grants-1983_04
ORD IDord-33e0326f897d4d1d825a00def4778bbc
Source noteuspto-grants-1983_04