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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy-HCID 74503—
Reactant4-Acetylphenylboronic acidHCID 3702122—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product7-(4-Acetylphenyl)-3-hydroxynaphthalene-2-carboxylic AcidHCID 5745704281.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-cb16a0ff8bd14ee693e79a2700529384
Source noteuspto-grants-2011_02