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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850366Generated: October 29, 2026

1-Indanylacetic acid → 3-(2-indanylacetyl)-L-thioproline ethyl ester

https://huagongshe.com/reaction/850366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Indanylacetic acidHCID 96501—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantEthyl (4R)-4-thiazolidinecarboxylateHCID 13011878—
SolventDichloromethaneHCID 6344—
Product3-(2-indanylacetyl)-L-thioproline ethyl esterHCID 13171691757.1%

Reaction Steps

While chilling with ice water, 1.4 g of 2-indanyl-acetic acid and 1.9 g of WSC.HCl were added to 15 ml of methylene chloride, and the mixture was stirred at room temperature for 5 minutes. Then, 1.3 g of L-thioproline ethyl ester dissolved in 10 ml of methylene chloride were added at room temperature, and the mixture was stirred further for 5 hours. The resultant liquid reaction mixture was washed with water, diluted hydrochloric acid and a saturated aqueous solution of sodium bicarbonate in that order. After an organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the resultant residue was subjected to column chromatography on silica gel, thereby obtaining 1.45 g (57%) of 3-(2-indanylacetyl)-L-thioproline ethyl ester in the form of colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017929
Source datasetuspto-grants-2000_01
ORD IDord-370bd9f2b83944b3b205113068c6438c
Source noteuspto-grants-2000_01