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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418865Generated: October 25, 2026

2-Bromonaphthalene → 4-(Naphthalen-2-yl)phenol

https://huagongshe.com/reaction/418865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromonaphthaleneHCID 11372—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant4-Hydroxyphenylboronic acidHCID 2734360—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(Naphthalen-2-yl)phenolHCID 2368682.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-bromonaphthalene (4.0 g, 19.32 mmol), 4-hydroxyphenylboronic acid (2.9 g, 21.24 mmol), potassium phosphate (14.35 g, 67.61 mmol), tricyclohexyl phosphine (542 mg, 1.93 mmol), toluene (80 mL) and water (4 mL) was added palladium acetate (217 mg, 0.965 mmol) under N2. The reaction mixture was heated to 100° C. for 24 h and then cooled to rt. Water was added and the mixture was extracted with EtOAc. The organic layer was separated, washed with water, brine, dried and concentrated to give crude product. Purification by column chromatography using 10% EtOAc in hexane afforded 105 mg of 4-naphthalen-2-yl-phenol. MS (ES) m/z: 220.07 (M) and 219.04 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093273B2
Source datasetuspto-grants-2012_01
ORD IDord-1ab526254d994016ab169b7a74efdca4
Source noteuspto-grants-2012_01