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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884718Generated: October 31, 2026

Potassium Phosphate, Tribasic → 2-(4-Hydroxyphenyl)naphthalene-1,4-dione

https://huagongshe.com/reaction/884718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1,4-Naphthalenedione, 2-bromo-HCID 74944—
ReactantTricyclohexylphosphineHCID 75806—
Reactant4-Hydroxyphenylboronic acidHCID 2734360—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(4-Hydroxyphenyl)naphthalene-1,4-dioneHCID 1177686945.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-bromo-1,4-naphthoquinone (1.0 g, 4.22 mmol), 4-hydroxyphenylboronic acid (640 mg, 4.64 mmol), potassium phosphate (3.135 g, 14.76 mmol), tricyclohexylphosphine (118 mg, 0.422 mmol), toluene (20 mL) and water (1 mL) was added palladium acetate (47 mg, 0.21 mmol) under N2. The reaction mixture was heated to 100° C. for 3 h. The reaction was cooled to rt and water was added. The mixture was extracted with EtOAc, and the combined organic extracts were washed with water and brine. The organic phase was separated, dried and concentrated to give crude product. Purification by column chromatography, using 10% EtOAc in hexane, gave 480 mg of 2-(4-hydroxy-phenyl)-[1,4]naphthoquinone (45%). MS (ES) m/z: 251.03 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242130B2
Source datasetuspto-grants-2012_08
ORD IDord-f3fd23c7f5a84b27899db9fc00c332a1
Source noteuspto-grants-2012_08