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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985425Generated: November 3, 2026

Methyl iodide → 5-Benzyloxy-1-methylindole-3-carboxaldehyde

https://huagongshe.com/reaction/1985425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-(phenylmethoxy)-1H-indole-3-carbaldehydeHCID 81398—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Benzyloxy-1-methylindole-3-carboxaldehydeHCID 12283854—

Reaction Steps

5g of 5-Benzyloxyindol-3-aldehyde was dissolved in 50 ml of N,N-dimethylformamide, and 0.84 g of 60% sodium hydride was added under ice-cooling. The reaction solution was stirred at room temperature for 30 minutes, 2.5 ml of methyl iodide was added and stirring was continued at room temperature for 16 hours. The reaction solution was cooled with ice, treated with water and ammonium chloride, and extracted with ethyl acetate and tetrahydrofuran. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was treated with diethyl ether and filtered, to give 4.6 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-bd079e0cfbdd467fb15f39e2bfe8729b
Source noteuspto-grants-2009_06