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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485343Generated: October 29, 2026

Ethyl Thioglycolate → 3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indole

https://huagongshe.com/reaction/485343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium hydrideHCID 24758—
ReactantN-(3-pyridyl)indole 3-propyl benzenesulfonateHCID 86740258—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indoleHCID 20270198—

Reaction Steps

A solution of 0.36 g of ethyl mercaptoacetate in 20 ml of dimethylformamide is treated with 0.145 g of a 50% oil dispersion of sodium hydride at room temperature under nitrogen for 15 minutes. A solution of 1.13 g of N-(3-pyridyl)indole-3-propyl benzenesulfonate in 5 ml of dimethylformamide is added at room temperature. The reaction mixture is stirred for 15 hours, diluted with 100 ml of water and extracted 4 times with 50 ml of ethyl ether. The organic extracts are washed with 50 ml of water and 20 ml of cold 1N hydrochloric acid. The acid phase is extracted with ether and brought to pH=8.5 with 50% sodium hydroxide solution. The aqueous phase is extracted with chloroform (3×30 ml). The chloroform extract is dried over potassium carbonate and evaporated to yield 3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indole; IR (CH2Cl2) 1725 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536505
Source datasetuspto-grants-1985_08
ORD IDord-521735bd8390406ea7297250b6ab968e
Source noteuspto-grants-1985_08