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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297353Generated: October 25, 2026

Methyl iodide → Methyl 1-methyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1297353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl indole-3-carboxylateHCID 589098—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-methyl-1H-indole-3-carboxylateHCID 84200696.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (60% dispersion in mineral oil, 8.56 g, 214.0 mmole) was added portionwise, allowing for gas evolution, to a solution of methyl 1H-indole-3-carboxylate (25.00 g, 142.7 mmole) in DMF (350 mL) at 0° C. When the NaH addition was complete, methyl iodide (44.4 mL, 713.5 mmole) was added at 0° C. The reaction was stirred at 0° C. for 15 minutes then at RT overnight. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were dried over K2CO3 and concentrated to afford the title compound (26.00 g, 96%) as an orange solid: MS (ES) m/e 190 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250424B2
Source datasetuspto-grants-2007_07
ORD IDord-57bb5209b7f64520afe125b22fee0872
Source noteuspto-grants-2007_07