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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922437Generated: October 29, 2026

Potassium Iodide → methyl 1-(3-methoxypropyl)-1H-indole-6-carboxylate

https://huagongshe.com/reaction/922437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetateHCID 8857—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
ReactantMethyl indole-6-carboxylateHCID 639844—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 1-(3-methoxypropyl)-1H-indole-6-carboxylateHCID 6754275882.2%

Reaction Steps

To a solution of methyl 1H-indole-6-carboxylate (5.0 g) in N,N-dimethylformamide (40 mL) was added dropwise a solution of 1-bromo-3-methoxypropane (5.24 g) in N,N-dimethylformamide (10 mL) under ice-cooling, and then thereto was added potassium iodide (948 mg), and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was sequentially added ethyl acetate and water under ice-cooling, and the organic layer was separated. The organic layer was washed with water twice and saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1→4/1) to give methyl 1-(3-methoxypropyl)-1H-indole-6-carboxylate [REx(6-1)] (5.8 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278944B2
Source datasetuspto-grants-2016_03
ORD IDord-c7a6004ce3b0481282c49eff9bdd8cb4
Source noteuspto-grants-2016_03