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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833551Generated: October 27, 2026

Water → Bis-[2-(3-methylindole-1-yl)ethyl]disulfide

https://huagongshe.com/reaction/1833551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(2-Bromoethyl)-3-methylindoleHCID 21389554—
SolventEthanolHCID 702—
ProductBis-[2-(3-methylindole-1-yl)ethyl]disulfideHCID 21389563—

Reaction Steps

A solution of 10.4 g. of sodium thiosulfate in 60 ml. of water and 100 ml. of ethanol is poured onto 8.6 g. of 1-(2-bromoethyl)-3-methylindole. The reaction mixture is stirred and heated at reflux for 3.5 hr., allowed to cool, and evaporated to dryness. The solid residue is dissolved in boiling isopropanol, dried with a hydrated alkali-aluminum silicate ("Molecular Sieves"), and filtered. Chilling of the filtrate causes 6.4 g. of the sodium indolyethyl thiosulfate derivative to precipitate. This material is collected by filtration and washed with ether. The isolated intermediate is heated at reflux with a solution of sodium hydroxide (9 g. of NaOH, 60 ml. of water, 140 ml. of ethanol) for 3 hr. Ethanol is removed under reduced pressure, the aqueous residue diluted with water and extracted with three portions of ether. Combined ether extracts are washed with water, saturated brine solution, and dried over magnesium sulfate. The filtrate is evaporated, to yield bis-[2-(3-methylindole-1-yl)ethyl]disulfide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066763
Source datasetuspto-grants-1978_01
ORD IDord-f38391849446497c8ba0f2e35f2e43ec
Source noteuspto-grants-1978_01