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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075786Generated: October 30, 2026

Indole → 3-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)-1H-indole hydroiodide

https://huagongshe.com/reaction/1075786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
ReactantEthylenethioureaHCID 2723650—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)-1H-indole hydroiodideHCID 86733373—

Reaction Steps

A mixture of 11.7 g indole in 100 ml methanol and 10.2 g 2-imidazolidinethione in 150 ml methanol is added to a well-stirred solution of 25.4 g iodine and 50 g potassium iodide in 100 ml water. The mixture is stirred for 2 hours at room temperature. The clear solution is concentrated in vacuo to one third of the original volume and cooled. The solid which separates is filtered off, dried and recrystallised from alcohol-ether to give 3-(2-imidazolin-2-ylthio)-indole hydriodide of the formula ##SPC9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954757
Source datasetuspto-grants-1976_05
ORD IDord-916e7c9e10e5428fbf74d51277c5e34f
Source noteuspto-grants-1976_05