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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215783Generated: November 1, 2026

Methyl iodide → 1-Methyl-5-methoxy-7-bromoindole

https://huagongshe.com/reaction/2215783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-5-methoxy-1H-indoleHCID 19804160—
SolventDimethylformamideHCID 6228—
Product1-Methyl-5-methoxy-7-bromoindoleHCID 21950018100.5%

Reaction Steps

To a suspension of sodium hydride (60%, 0.32 g, 7.96 mmol) in DMF (18 mL) was added a solution of 5-methoxy-7-bromoindole (1.5 g, 6.63 mmol) in DMF (25 mL). The mixture was stirred at room temperature for 1 h, and then methyl iodide (0.62 mL, 9.95 mmol) was added with cooling in an ice-water-bath. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with water and extracted with ethyl acetate. The extract was washed with water and brine, dried (sodium sulfate) and concentrated to give a crude product (1.6 g, 100%), which was used without further purification. 1HNMR (400 MHz, CDCl3) 3.82 (s, 3H), 4.10 (s, 3H), 6.36 (d, J=3.13 Hz, 1H), 6.96 (d, J=2.74 Hz, 1H), 7.0 (d, J=2.35 Hz, 1H), 7.03 (d, J=2.35 Hz, 1H); MS (ES, m/z): C10H10BrNO: 240.08 (M+(79Br)+1), 242.1 (M+(81Br)+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109229B2
Source datasetuspto-grants-2006_09
ORD IDord-3e7ae3a564854850ad0a73ba011b4bd4
Source noteuspto-grants-2006_09