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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581113Generated: October 26, 2026

Benzyl Bromide → 4-methoxy-2-methyl-1-(phenylmethyl)-1H-indole

https://huagongshe.com/reaction/581113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
Reactant4-methoxy-2-methyl-1H-indoleHCID 10773274—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-methoxy-2-methyl-1-(phenylmethyl)-1H-indoleHCID 1077714784%

Reaction Steps

4-Methoxy-2-methyl-1H-indole (1 g, 6.2 mmol) was added to 248 mg (6.2 mmol) of 60% sodium hydride/mineral oil (washed with hexane before adding DMF) in 15 mL of DMF and after stirring for 0.5 hours 0.74 mL (6.2 mmol) of benzyl bromide was added. The mixture was stirred at room temperature for 18 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with brine, dried (MgSO4) and after concentrating at reduced pressure, the residue was chromatographed on silica gel eluting with 20% EtOAc/hexane to give 1.3 g (84% yield) of 4-methoxy-2-methyl-1-(phenylmethyl)-1H-indole, melting at 96-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919810
Source datasetuspto-grants-1999_07
ORD IDord-c0842cf3021c4a0c95de02c1051a69ad
Source noteuspto-grants-1999_07