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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281744Generated: October 26, 2026

Methyl iodide → 1,6-Dimethyl-4-iodo-indole-3-carboxaldehyde

https://huagongshe.com/reaction/1281744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-Methyl-4-iodo-indole-3-carboxaldehydeHCID 22605374—
SolventDimethylformamideHCID 6228—
Product1,6-Dimethyl-4-iodo-indole-3-carboxaldehydeHCID 22605373—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold solution (0° C.) of 6-methyl-4-iodo-indole-3-carboxaldehyde (265 mg, 0.92 mmol) in dry DMF (2 mL) was added NaH (60% dispersion in mineral oil, 50 mg, 1.25 mmol). The resulting mixture was stirred at 0° C. for 20 min. Iodomethane (0.5 mL, excess) was added to the reaction mixture in a drop wise fashion. The cooling bath was removed and the resulting mixture was stirred at room temperature for 1.5 h. The mixture was quenched with water and was extracted repeatedly from EtOAc. Combined organic was washed with water (twice) and brine. After drying over magnesium sulfate, solvent was removed. The product, 1,6-dimethyl-4-iodo-indole-3-carboxaldehyde was obtained as a solid was which was suspended in hexane, stirred for few minutes and was filtered. The product was further washed with more hexane and was dried to yield 213 mg (77%) of the desired product. MS: 300 (M+H), 322 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455525B1
Source datasetuspto-grants-2002_09
ORD IDord-f9ba34dfdcca41e7aa947541bf346de0
Source noteuspto-grants-2002_09