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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064717Generated: October 26, 2026

Water → (3-Fluorophenyl)(4-hydroxyphenyl)methanone

https://huagongshe.com/reaction/1064717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron tribromideHCID 25134—
Reactant(3-Fluorophenyl)(4-methoxyphenyl)methanoneHCID 13467539—
SolventDichloromethaneHCID 6344—
Product(3-Fluorophenyl)(4-hydroxyphenyl)methanoneHCID 1135636374%

Reaction Conditions

Temperature25 °C

Reaction Steps

(3-fluorophenyl)(4-methoxyphenyl)methanone (1.0 g, 4.34 mmol) in 50 mL DCM at −78° C. while stirring was treated with 1M boron tribromide (13.03 mL, 13.03 mmol) dropwise over 20 minutes. The mixture was allowed to warm to 25° C. and stir for 18 hours. The mixture was treated with water (1 mL) and stirred for 5 minutes, followed by additional water (2 mL) and stirred for 10 minutes, and finally treated with more water (50 mL) and stirred for 20 minutes. The mixture was then extracted with DCM (50 mL ×2). The organic layers were combined, dried, filtered, and the filtrate evaporated under reduced pressure. The residue was purified by flash chromatography to provide the title compound (0.69 g, 74% yield). 1HNMR (300 MHz, CD3OD) δ 6.92 (d, 2H, J=8.9 Hz), 7.26 (m, 1H), 7.41-7.58 (m, 3H), 7.79 (d, 2H, J=8.9 Hz); MS (DCI) m/z 217 (M+H)+, 234 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-75422897c38e454997d3ede61265864b
Source noteuspto-grants-2005_11