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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057129Generated: October 30, 2026

Ethanethiol → HCID 86596561, compound

https://huagongshe.com/reaction/2057129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 11470406HCID 11470406—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 86596561HCID 86596561—

Reaction Steps

In 200 ml of acetonitrile was dissolved 10 g of (4R)-2-oxo-3-benzylthiazolidin-4-carboxylic acid, and 9.2 g of dicyclohexylcarbodiimide was added to the solution under room temperature. Subsequently, to the solution were added 3.3 ml of ethanethiol, and 670 mg of 4-dimethylaminopyridine in this order under ice-cooling, and the mixture was stirred at room temperature for 2 hours. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane:ethyl acetate=10:1) to give 10.8 g of (4S)-4-ethylthiocarbonyl-3-benzylthiazolidin-2-one as oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335778B2
Source datasetuspto-grants-2008_02
ORD IDord-d69cdcd809f44e02a24b6273812ae565
Source noteuspto-grants-2008_02