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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1,4-Naphthalenedione, 2-bromo- | HCID 74944 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Hydroxyphenyl)naphthalene-1,4-dione | HCID 11776869 | 45.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242130B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-f3fd23c7f5a84b27899db9fc00c332a1 |
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| Source note | uspto-grants-2012_08 |
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