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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657746Generated: October 27, 2026

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

https://huagongshe.com/reaction/1657746

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 reactionmixture 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 numberUS03962236
Source datasetuspto-grants-1976_06
ORD IDord-4ba59820066b48328aa98abb1b556bb2
Source noteuspto-grants-1976_06