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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835205Generated: October 30, 2026

Water → 5-methoxy-1-methyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/1835205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Methoxyindole-3-carbaldehydeHCID 82758—
SolventDimethylformamideHCID 6228—
Product5-methoxy-1-methyl-1H-indole-3-carbaldehydeHCID 925973—

Reaction Steps

A solution of 5-methoxyindole-3-carboxaldehyde (80 g) in dimethylformamide (1 L) under nitrogen was treated portion-wise with sodium hydride (20.1 g, 60% dispersion in mineral oil) over 15 minutes. After stirring at ambient temperature for 30 minutes the mixture was treated dropwise with methyl iodide (31.3 mL) over 10 minutes and stirring was then continued for a further 2 hours. The reaction mixture was poured cautiously into water then extracted with ethyl acetate. The organic phase was washed with water, then dried over sodium sulfate and then evaporated. The residue was triturated with pentane to give the title compound (76 g) as a pale brown solid, m.p. 133-134° C. 1H NMR [(CD3)2SO]: δ 9.86 (1H, s); 8.20 (1H, s); 7.60 (1H, d, J=2.6 Hz); 7.50 (1H, d, J=8.9 Hz); 6.96 (1H, dd, J=8.9 and 2.6 Hz); 3.86 and 3.80 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770643B2
Source datasetuspto-grants-2004_08
ORD IDord-61799e4d9eb342648c68524457553ba7
Source noteuspto-grants-2004_08