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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086265Generated: October 31, 2026

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

https://huagongshe.com/reaction/1086265

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

1.4 g of 2-indanylacetic acid and 1.9 g of WSC.HCl were added to 15 ml of methylene chloride under ice-cooling. The mixture was stirred for 5 minutes at room temperature. After an addition of 1.3 g of L-thioproline ethyl ester dissolved in 10 ml of methylene chloride, the mixture was stirred for 5 hours. The reaction mixture was washed with water, diluted hydrochloric acid, and saturated sodium hydrogen carbonate in this order. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue thus obtained was purified by silica gel column chromatography to produce 1.45 g of 3-(2-indanylacetyl)-L-thioproline ethyl ester as a colorless oil (yield: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028604
Source datasetuspto-grants-1991_07
ORD IDord-a430a8c68ecf419ba0434ab8f081b75b
Source noteuspto-grants-1991_07