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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368994Generated: November 1, 2026

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

https://huagongshe.com/reaction/1368994

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 numberUS06576654B1
Source datasetuspto-grants-2003_06
ORD IDord-4be2d2c1e5394a639567097a33e15ea2
Source noteuspto-grants-2003_06