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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795189Generated: November 2, 2026

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

https://huagongshe.com/reaction/1795189

Reaction equation

Participants

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

Reaction Steps

3.1 g (11.7 mmol) of 2-ethyl-4-methoxy-1-(phenylmethyl)-1H-indole is O-demethylated by treating it with 48.6 mL of 1M BBr3/CH2Cl2, then stirred at room temperature for 5 hours and concentrated at reduced pressure. The residue is dissolved in ethyl acetate, then washed with brine and dried. The reaction product is then chromatographed on silica gel (eluted 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 numberUS07026348B2
Source datasetuspto-grants-2006_04
ORD IDord-0b6057a2820c41c192d8b260cf8f7b5e
Source noteuspto-grants-2006_04