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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215789Generated: November 3, 2026

Methyl iodide → 7-Bromo-5-fluoro-1-methyl-1H-indole

https://huagongshe.com/reaction/2215789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant7-bromo-5-fluoro-1H-indoleHCID 3852879—
SolventDimethylformamideHCID 6228—
Product7-Bromo-5-fluoro-1-methyl-1H-indoleHCID 21950063—

Reaction Steps

To a suspension of sodium hydride (60%, 1.75 g, 43.8 mmol) in DMF (134 mL) was added a solution of 5-fluoro-7-bromoindole (7.8 g, 36.4 mmol) in DMF (10 mL). After 1 h at room temperature, the mixture was treated with methyl iodide (3.4 mL, 54.6 mmol) with cooling in an ice-water bath. The reaction mixture was allowed to warm up room temperature and stirred overnight. The reaction was quenched with water, extracted with ethyl acetate, and the organic layer was washed with water and brine, dried (sodium sulfate) and concentrated to give a crude product, which was used without further purification. 1H NMR (400 MHz, CDCl3) 4.06 (s, 3H), 6.34 (d, J=3.13 Hz, 1H), 6.96 (d, J=3.13 Hz, 1H), 7.07 (dd, J1=2.34 Hz, J2=8.60 Hz, 1H), 7.12 (dd, J1=2.34 Hz, J2=9.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109229B2
Source datasetuspto-grants-2006_09
ORD IDord-f968cbe16e6748b1bc6bcf5d7126b312
Source noteuspto-grants-2006_09