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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702214Generated: November 2, 2026

(2S)-3-benzoylthio-2-methylpropionyl chloride → tert.-butyl (4S)-1-benzyl-3-[(2S)-3-benzoylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylate

https://huagongshe.com/reaction/1702214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-3-benzoylthio-2-methylpropionyl chlorideHCID 12878434—
Reactanttert-butyl (S)-1-benzyl-2-oxoimidazolidine-4-carboxylateHCID 13053983—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Producttert.-butyl (4S)-1-benzyl-3-[(2S)-3-benzoylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylateHCID 1319317276.6%

Reaction Steps

27.6 g of tert.-butyl (4S)-1-benzyl-2-oxo-imidazolidine-4-carboxylate, 11.2 g of potassium tert.-butoxide, (2S)-3-benzoylthio-2-methylpropionyl chloride (prepared from 22.4 g of (2S)-3-benzoylthio-2-methylpropionic acid and 25 ml of thionyl chloride) and 200 ml of tetrahydrofuran are treated in the same manner as described in Example 2-(2). Then, the oily residue obtained is purified by silica gel chromatography (Solvent, toluene-ethyl acetate(20:1)) and triturated with n-hexane. 34.1 g of tert.-butyl (4S)-1-benzyl-3-[(2S)-3-benzoylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylate are obtained as colorless crystals. Yield: 70.7%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380644
Source datasetuspto-grants-1983_04
ORD IDord-8db01cf9033e41d0806f2632996cc33d
Source noteuspto-grants-1983_04