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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868839Generated: October 29, 2026

Methyl iodide → HCID 86665673, compound

https://huagongshe.com/reaction/868839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 2762435HCID 2762435—
SolventAcetonitrileHCID 6342—
ProductHCID 86665673HCID 86665673—

Reaction Steps

Dimethyl-(4-methyl-1H-indol-3-ylmethyl)-amine (20 g, 98 mmol) is suspended in acetonitrile, and warmed to completely dissolve the material. The reaction is cooled to room temperature and then methyl iodide (9.1 mL, 147 mmol) is added dropwise to the reaction. The reaction is covered with foil and then stirred at room temperature overnight. The reaction is then filtered and the filtrate evaporate in vacuo to give an oil that is taken up in acetonitrile. The white solid is then triturated with acetonitrile and ether, and combined with the original solid to give the title compound that is used without further purification (30 g, 87 mmol, 88%) LC/MS (M++1): 347.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969348B2
Source datasetuspto-grants-2015_03
ORD IDord-506eb8760e4b4118a2a54488280a975a
Source noteuspto-grants-2015_03