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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3383Generated: October 27, 2026

Benzyl Bromide → 2-ethyl-5-methoxy-1-(phenylmethyl)-1H-indole

https://huagongshe.com/reaction/3383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant2-ethyl-5-methoxy-1H-indoleHCID 10702405—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-ethyl-5-methoxy-1-(phenylmethyl)-1H-indoleHCID 1051583682%

Reaction Steps

2-Ethyl-5-methoxy-1H-indole (5.6 g, 21.5 mmol) was dissolved in 150 mL of DMF and 20 mL of THF and 1.0 g (25 mmol) of 60% sodium hydride was added. After stirring for 0.17 hours, 3.0 mL (25 mmol) of benzyl bromide was added. The mixture was stirred at room temperature for 10 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with water, saturated NaCl solution, and dried (Na2 SO4). The EtOAc was evaporated and the residue was chromatographed on silica gel eluting with a gradient, 5% EtOAc/hexane→15% EtOAc/hexane to give 4.6 g (82% yield) of 2-ethyl-5-methoxy-1-(phenylmethyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733923
Source datasetuspto-grants-1998_03
ORD IDord-58e3159b6ca6432dae5a788f94e6f3a6
Source noteuspto-grants-1998_03