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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732311Generated: October 26, 2026

4-Thiazolidinecarboxylic acid, 2-ethyl- → HCID 21162278, compound

https://huagongshe.com/reaction/1732311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Thiazolidinecarboxylic acid, 2-ethyl-HCID 98344—
ReactantEthanethioic acid, S-(3-chloro-2-methyl-3-oxopropyl) esterHCID 103458—
SolventSodium HydroxideHCID 14798—
ProductHCID 21162278HCID 21162278—

Reaction Steps

3-Acetylthio-2-methylpropanoic acid chloride (5.4 g. prepared from 3-acetylthio-2-methylpropanoic acid and thionyl chloride, b.p. 80°) and 2 N sodium hydroxide (15 ml.) are added to a solution of 2-ethyl-4-thiazolidinecarboxylic acid [Z.Naturforschg, 17b, 765 (1962)] (5.2 g.) in normal sodium hydroxide (30 ml.) chilled in an ice-water bath. After three hours stirring at room temperature, the mixture is extracted with ether, the aqueous phase is acidified and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated to dryness in vacuo to yield 3-(3-acetylthio-2-methylpropanoyl)-2-ethyl-4-thiazolidinecarboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237134
Source datasetuspto-grants-1980_12
ORD IDord-bd4f8f92b2e04bff874ebcdc998e9130
Source noteuspto-grants-1980_12