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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397857Generated: October 30, 2026

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

https://huagongshe.com/reaction/397857

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 is stirred at room temperature for 5 hours and concentrated at reduced pressure. The residue is dissolved in ethyl acetate, washed with brine and dried (MgSO4). After concentrating at reduced pressure, the residue is 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 numberUS06610728B2
Source datasetuspto-grants-2003_08
ORD IDord-055ae6b8605143e38b01cdc39d18da22
Source noteuspto-grants-2003_08