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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795188Generated: November 2, 2026

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

https://huagongshe.com/reaction/1795188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-ethyl-4-methoxy-1H-indoleHCID 9855607—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
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/minerial 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 and extracted 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 numberUS07026348B2
Source datasetuspto-grants-2006_04
ORD IDord-58813b829f9c4daca08f9a2e01027093
Source noteuspto-grants-2006_04