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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276473Generated: October 31, 2026

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

https://huagongshe.com/reaction/1276473

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) was dissolved in 30 mL of DMF and 960 mg (24 mmol) of 60% NaH/minerial oil was added. After 1.5 hours, 2.9 mL(24 mmol) of benzyl bromide was added. After 4 hours, the mixture was diluted with water and extracted twice with ethyl acetate. The combined ethyl acetate was washed with brine, dried (MgSO4) and concentrated at reduced pressure. The residue was 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 numberUS06166062
Source datasetuspto-grants-2000_12
ORD IDord-8337e9af252d483d93581e6e03a33a40
Source noteuspto-grants-2000_12