HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361008Generated: October 29, 2026
Sodium Carbonate → 7-(4-Acetylphenyl)-3-hydroxynaphthalene-2-carboxylic Acid
https://huagongshe.com/reaction/1361008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy- | HCID 74503 | — |
| Reactant | 4-Acetylphenylboronic acid | HCID 3702122 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(4-Acetylphenyl)-3-hydroxynaphthalene-2-carboxylic Acid | HCID 57457042 | 81.2% |
Reaction Steps
To 7-bromo-3-hydroxynaphthalene-2-carboxylic acid (100 mg, 0.37 mmol) (example 340) was added a solution of 4-acetylphenylboronic acid (92 mg, 0.56 mmol) in acetone (2.2 mL) followed by a solution of sodium carbonate (198 mg, 1.87 mmol) in water (3.3 mL). A suspension of palladium(II) acetate (4 mg, 0.02 mmol) in acetone (0.5 mL) was filtered and added to the above solution. The mixture was purged with N2 and stirred vigorously for 24 hours at room temperature. The reaction mixture was poured into 1 N hydrochloric acid (aq.) (60 mL) and the precipitate was filtered off and rinsed with water (3×40 mL). The crude product was dissolved in acetone (25 mL) and dried with magnesium sulfate (1 h). Filtration followed by concentration furnished the title compound as a solid (92 mg). 1H-NMR (DMSO-d6): δ 12.60 (1H, bs), 8.64 (1H, s), 8.42 (1H, s), 8.08 (2H, d), 7.97 (2H, d), 7.92 (2H, m), 7.33 (1H, s), 2.63 (3H, s); HPLC-MS (Method (A): m/z: 307 (M+1); Rt=3.84 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07879893B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-cb16a0ff8bd14ee693e79a2700529384 |
|---|
| Source note | uspto-grants-2011_02 |
|---|