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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836658Generated: October 31, 2026

Boron tribromide → 6-Hydroxyindole

https://huagongshe.com/reaction/1836658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant6-Methoxy-1H-indoleHCID 76659—
SolventDichloromethaneHCID 6344—
Product6-HydroxyindoleHCID 524508—

Reaction Steps

6-Methoxyindole (1.47 g, 10.00 mmol) was cooled to 0° C. in methylene chloride and BBr3 (2 M in methylene chloride, 25 mL, 50.00 mmol) was added. After stirring 16 h at room temperature, TLC analysis indicated the reaction was complete. The reaction was quenched with water and the layers separated. The organic layers were washed with 1 N NaOH. The basic aqueous layers were acidified with conc. HCL, extracted with methylene chloride, dried over anhydrous magnesium sulfate, and concentrated in vacuo to give the crude 6-hydroxyindole which was used directly for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777437B2
Source datasetuspto-grants-2004_08
ORD IDord-99b017107f31491986d9e36245860446
Source noteuspto-grants-2004_08