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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243157Generated: October 26, 2026

Water → 1-(4-hydroxyphenyl)-1H-indole

https://huagongshe.com/reaction/2243157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron tribromideHCID 25134—
Reactant1-(4-methoxyphenyl)-1H-indoleHCID 775715—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product1-(4-hydroxyphenyl)-1H-indoleHCID 1665567226.8%

Reaction Steps

To 2.90 g (13 mmol) 1-(4-methoxyphenyl)-1H-indole in 80 ml anhydrous DCM at −78° C. was added 2.27 ml (24 mmol) BBr3. The solution was allowed to gradually warm to room temperature overnight. The solution was poured into a slurry of ice and water. Brine was added and the product was extracted with ethyl acetate. The organic phase was dried over MgSO4 and concentrated. The crude product was chromatographed on SiO2 to afford 0.73 g 1-(4-hydroxyphenyl)-1H-indole as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674818B2
Source datasetuspto-grants-2010_03
ORD IDord-22446ecb096948f2a60bcd2d0fd49a53
Source noteuspto-grants-2010_03