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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702203Generated: October 31, 2026

Trifluoroacetic acid → (4S)-1-methyl-3-[(2S)-3-acetylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylic acid

https://huagongshe.com/reaction/1702203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert.-butyl (4S)-1-methyl-3-[(2S)-3-acetylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylateHCID 13053996—
Product(4S)-1-methyl-3-[(2S)-3-acetylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylic acidHCID 1305399499.5%

Reaction Steps

A mixture of 0.72 g of tert.-butyl (4S)-1-methyl-3-[(2S)-3-acetylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylate and 3.5 ml of trifluoroacetic acid is stirred at room temperature for one hour. Then, the reaction mixture is treated in the same manner as described in Example 1-(5). 0.6 g of (4S)-1-methyl-3-[(2S)-3-acetylthio-2-methylpropionyl]-2-oxo-imidazolidine-4-carboxylic acid is obtained as colorless syrup. Yield: quantitative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380644
Source datasetuspto-grants-1983_04
ORD IDord-db923aa977e74b47b300356e9a85ab93
Source noteuspto-grants-1983_04