HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700870Generated: November 1, 2026
Potassium Carbonate → 4,4'-Difluorobenzophenone
https://huagongshe.com/reaction/1700870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,4'-Difluorobenzhydryl alcohol | HCID 123049 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Product | 4,4'-Difluorobenzophenone | HCID 9582 | 98.5% |
Reaction Steps
A schlenk tube containing the mixture of 4,4′-Diflourobenzhydrol (220 mg, 1.0 mmol), K2CO3 (276 mg, 2.0 mmol), Pd(dba)2 (6 mg, 10 μmol) and ligand 1 (10 mg, 30 μmol) was degassed thoroughly under vacuum and purged with Ar. Chlorobenzene (0.15 mL) and toluene (4 mL) were added to the schlenk. The mixture was heated at 105° C. for 12 h. The reaction was taken up in ether (100 mL) and washed with H2O (30 mL) and brine (30 mL). The organic phase was dried over MgSO4, filtered and concentrated under vacuum. The crude product was purified by column chromatography on silica gel using hexanes/ethyl acetate as elute to afford compound A as an off-white solid (215 mg, 98%) after drying under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350916B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-716356e6eaf64f07b214a95527b48cbf |
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| Source note | uspto-grants-2002_02 |
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