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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383860Generated: November 2, 2026

Methyl iodide → 3-Bromo-5-chloro-1-methyl-1H-indole

https://huagongshe.com/reaction/2383860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-bromo-5-chloro-1H-indoleHCID 2762968—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product3-Bromo-5-chloro-1-methyl-1H-indoleHCID 6878742765%

Reaction Steps

K2CO3 (1.39 g, 10.08 mmol) was added to a stirred solution of 3-bromo-5-chloro-1H-indole (775 mg, 3.36 mmol) in DMF (7.5 mL) and the resulting mixture was stirred for 30 minutes. This was followed by the addition of methyl iodide (572.5 mg, 4.03 mmol) at 0-5° C. and the stirring was continued for a further 2 hours at room temperature. The reaction was monitored by TLC (10% ethylacetate in hexane). The reaction mixture was partitioned between ice water and DCM. The organic layer was concentrated to afford the crude product. Purification by column chromatography on silica gel (5% ethylacetate in hexane) afforded 530 mg of 3-Bromo-5-chloro-1-methyl-1H-indole (65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-82d23f9c250545f3972548757148d254
Source noteuspto-grants-2012_09