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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303522Generated: October 31, 2026

Benzyl Bromide → 1-benzyl-5-methoxy-1h-indole

https://huagongshe.com/reaction/2303522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant5-MethoxyindoleHCID 13872—
ReactantSodium hydrideHCID 24758—
Product1-benzyl-5-methoxy-1h-indoleHCID 261406—

Reaction Steps

5-Methoxy-1H-indole (5.6 g, 21.5 mmol) was reacted with 1.0 g (25 mmol) of 60% sodium hydride and then 3.0 mL (25 mmol) of benzyl bromide by the method described in Example 12, Part D to give crude 5-methoxy-1-(phenylmethyl)-1H-indole. This material was dissolved in 250 mL of methylene chloride, cooled to −5° C., 50 mL of 1M BBr3/CH2Cl2 added, the cooling bath removed and the mixture stirred for 1.75 hours. Ice water was added and the mixture stirred. The organic layer was separated, washed with saturated NaCl, dried (Na2SO4), and concentrated at reduced pressure. The residue was chromatographed on silica gel and eluted with 20% ether/hexaneØether to give 870 mg (19% overall yield) of crude 5-hydroxy-1-(phenylmethyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433001B1
Source datasetuspto-grants-2002_08
ORD IDord-3986279546064e8a8623842f7f4e9b2f
Source noteuspto-grants-2002_08