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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280814Generated: November 2, 2026

1-Benzyl-2-ethyl-4-methoxy-1H-indole → 1-Benzyl-2-ethyl-1H-indol-4-OL

https://huagongshe.com/reaction/1280814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-2-ethyl-4-methoxy-1H-indoleHCID 9943241—
ReactantBoron tribromide dichloromethaneHCID 22277759—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-2-ethyl-1H-indol-4-OLHCID 981641654%

Reaction Steps

A solution of 3.1 g (11.7 mmol) of 2-ethyl-4-methoxy-1-(phenylmethyl)-1H-indole and 48.6 mL of 1M BBr3/CH2Cl2 in 50 mL of methylene chloride was stirred at room temperature for 5 hours and concentrated at reduced pressure. The residue was dissolved in ethyl acetate, washed with brine and dried (MgSO4). After concentrating at reduced pressure, the residue was chromatographed on silica gel eluting with 20% EtOAc/hexane to give 1.58 g (54% yield) of 2-ethyl-4-hydroxy-1-(phenylmethyl)-1H-indole, mp, 86-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451839B1
Source datasetuspto-grants-2002_09
ORD IDord-3dd8eb1bb81c4f82ba102f806f946f21
Source noteuspto-grants-2002_09