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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741132Generated: November 1, 2026

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

https://huagongshe.com/reaction/1741132

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/mineral 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 numberUS05972988
Source datasetuspto-grants-1999_10
ORD IDord-c1e7c8e6cd224226850855e2cba4f2ea
Source noteuspto-grants-1999_10