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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952724Generated: November 4, 2026

Methyl iodide → 1-(1-Methyl-1H-indol-3-yl)ethanone

https://huagongshe.com/reaction/1952724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3-AcetylindoleHCID 12802—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Methyl-1H-indol-3-yl)ethanoneHCID 594156—

Reaction Steps

3-Acetyl-1H-indole (4.00 g, 0.025 mol) was dissolved in dry THF (100 ml), and treated with 80% sodium hydride (0.794 g, 0.0263 mol) with stirring under Ar. After 0.5 h, methyl iodide (2.36 ml, 0.038 mol) was added. After 20 h, the reaction mixture was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The organic layer was then dried (Na2SO4), and evaporated under reduced pressure to give the title compound as a pale brown oil which crystallised on standing (4.20 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114329
Source datasetuspto-grants-2000_09
ORD IDord-5289338f8f8d4baca79632ba92c4e035
Source noteuspto-grants-2000_09