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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36894Generated: October 29, 2026

Methyl iodide → HCID 54508469, compound

https://huagongshe.com/reaction/36894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactantsodium 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioateHCID 23695420—
SolventEthanolHCID 702—
ProductHCID 54508469HCID 54508469—

Reaction Steps

A solution of sodium 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioate (3 g, prepared in the previous Example) and methyl iodide (0.5 ml) in 95% ethanol (15 ml) is refluxed for one hour. The orange reaction mixture is concentrated, taken up with ether and washed with water. The organic phase is dried over sodium sulfate and concentrated. After chromatography on silica gel (eluent: cyclohexane/AcOEt 70/30), methyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioate (13 g) is obtained in the form of an oil, which is taken up with pentene to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418242
Source datasetuspto-grants-1995_05
ORD IDord-4a8537d9c43449d3a739c166cafcbc0e
Source noteuspto-grants-1995_05