HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418880Generated: October 26, 2026
Sodium Carbonate → 3-(4-hydroxyphenyl)-4H-chromen-4-one
https://huagongshe.com/reaction/418880
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Bromochromone | HCID 521256 | — |
| Reactant | Pyridinium hydrochloride | HCID 21584435 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(4-hydroxyphenyl)-4H-chromen-4-one | HCID 10966551 | 83% |
Reaction Steps
To a mixture of 3-bromochromone (1.5 g, 6.66 mmol), 4-methoxy phenyl boronic acid (1.01 g, 6.66 mmol), sodium carbonate (2.12 g, 20.0 mmol), toluene (40 mL) and water (10 mL) was added tetrakis-triphenyl phosphine palladium (385 mg, 0.33 mmol) under N2. The reaction mixture was heated to 110° C. for 5 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, which was purified by column chromatography, using 20% EtOAc in hexane to give, 885 mg of 4′-methoxychromone product in 52% yield. A mixture of the above mentioned 4′-methoxychromone (400 mg, 1.58 mmol) and pyridinium hydrochloride (5 g) was heated at 190° C. for 4 h. The reaction mixture was cooled to rt, diluted with water, neutralized with NaHCO3 and filtered to give 314 mg of 3-(4-hydroxyphenyl)-4H-chromen-4-one (83%). MS (ES) m/z: 239.95 (M+1), 238.99 (M); Mp. 237-238° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093273B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-bcd9cf6583cc4586a5ab924fce839190 |
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| Source note | uspto-grants-2012_01 |
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