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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368993Generated: October 30, 2026

Benzyl Bromide → 1-Benzyl-2-ethyl-4-methoxy-1H-indole

https://huagongshe.com/reaction/1368993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-ethyl-4-methoxy-1H-indoleHCID 9855607—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-2-ethyl-4-methoxy-1H-indoleHCID 994324149%

Reaction Steps

2-Ethyl-4-methoxy-1H-indole (4.2 g, 24 mmol) is dissolved in 30 mL of DMF and 960 mg (24 mmol) of 60% NaH/mineral oil is added. After 1.5 hours, 2.9 mL(24 mmol) of benzyl bromide is added. After 4 hours, the mixture is diluted with water extracting twice with ethyl acetate. The combined ethyl acetate is washed with brine, dried (MgSO4) and concentrated at reduced pressure. The residue is chromatographed on silica gel and eluted with 20% EtOAc/hexane to give 3.1 g (49% yield) of 2-ethyl-4-methoxy-1-(phenylmethyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576654B1
Source datasetuspto-grants-2003_06
ORD IDord-b8189b0dde7946118fcd5647be56b54f
Source noteuspto-grants-2003_06