HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596953Generated: October 27, 2026
Water → Bis-[2-(3-methylindole-1-yl)ethyl]disulfide
https://huagongshe.com/reaction/596953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1-(2-Bromoethyl)-3-methylindole | HCID 21389554 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Bis-[2-(3-methylindole-1-yl)ethyl]disulfide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04012511 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-5390b61ab5b648b8a90c7e3f2b8bc5ad |
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| Source note | uspto-grants-1977_03 |
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