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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711827Generated: November 3, 2026

Methyl iodide → 1-methyl-1H-indole-5-carbaldehyde

https://huagongshe.com/reaction/1711827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantIndole-5-carboxaldehydeHCID 589040—
SolventDimethylformamideHCID 6228—
Product1-methyl-1H-indole-5-carbaldehydeHCID 753753491%

Reaction Steps

To a solution of indole-5-carbaldehyde (1.0 g, 6.9 mmol) in DMF (15 mL) was added sodium hydride (303 mg of 60% dispersion in oil, 7.59 mmol) in 3 portions. The mixture was stirred for 30 mins. Methyl iodide (1.96 g, 13.8 mmol) was then added and the mixture was stirred overnight. Ethyl acetate (200 mL) was added and solution was washed with H2O (3×20 mL) and brine (25 mL) dried over MgSO4 and concentrated to afford N-methylindole-5-carboxaldehyde as an orange oil (1.0 g, 91%). 1H NMR (200 MHz, CDCl3) δ 10.05 (s, 1H), 8.09 (s, 1H), 7.90-7.80 (m, 1H), 7.35-7.15 (m, 2H), 6.85-6.80 (m, 1H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-6abd47f315b84f009ceec7f73c875dcf
Source noteuspto-grants-2010_09