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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791589Generated: November 3, 2026

Water → 2-methyl-1H-indol-5-ol

https://huagongshe.com/reaction/1791589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBoron tribromideHCID 25134—
Reactant5-Methoxy-2-methylindoleHCID 70642—
SolventDichloromethaneHCID 6344—
Product2-methyl-1H-indol-5-olHCID 8333693%

Reaction Conditions

Temperature-45 °C

Reaction Steps

A solution of boron tribromide (32.5 ml, 341 mmol) in methylene choride (60 ml) was added in portions to a solution of 5-methoxy-2-methylindole (25 g, 155 mmol) in methylene chloride (250 ml) cooled at −45° C. After stirring for 15 minutes at −30° C., the mixture was warmed up to ambient temperature and stirred for 1 hour. Methylene chloride (300 ml) was added in portions and the mixture was cooled to 0° C. Water was added in portions and the mixture was adjusted to pH6 with 4N sodium hydroxide. The organic layer was separated. The aqueous layer was extracted with methylene chloride and the organic layers were combined, washed with water, brine, dried (MgSO4) and the volatiles were removed by evaporation. The residue was purified by column chromatography eluting with ethyl acetate/methylene chloride (1/9 followed by 15/85) to give 5-hydroxy-2-methylindole (21.2 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-c969e0ea9f6645219c26c1d9c55db636
Source noteuspto-grants-2006_07