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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215752Generated: October 30, 2026

Methyl iodide → 7-Bromo-1-methyl-1H-indole

https://huagongshe.com/reaction/2215752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant7-BromoindoleHCID 2757020—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-Bromo-1-methyl-1H-indoleHCID 21950069—

Reaction Steps

A 60% dispersion of sodium hydride in mineral oil (1.40 g, 97 mmol) was washed with hexanes (3×10 mL, 1×5 mL), suspended in THF (50 mL) and CH3I added (1.64 mL, 26.3 mmol) followed by a solution of 7-bromoindole (4.06 g, 20.7 mmol) in THF (15 mL), with vigorous gas evolution. After 1 h at rt, the mixture was treated with additional CH3I (0.28 mL, 4.5 mmol) and stirred overnight. Saturated aq NaHCO3 was added and the mixture poured into EtOAc, which was separated, washed with saturated aq NaHCO3, dried (MgSO4) and concentrated to afford 1-methyl-7-bromoindole as an off-white semisolid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109229B2
Source datasetuspto-grants-2006_09
ORD IDord-77eeff928b9342fe89df7a6ccbcc8bbb
Source noteuspto-grants-2006_09