HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40468Generated: October 25, 2026
Potassium Phosphate, Tribasic → HCID 58502816, compound
https://huagongshe.com/reaction/40468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Bromo-3-methoxycyclopent-2-enone | HCID 11095426 | — |
| Reactant | 4'-Chloro-4-ethylbiphenyl-3-ylboronic acid | HCID 59445927 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Product | HCID 58502816 | HCID 58502816 | 75.5% |
Reaction Steps
To a stirred suspension of 2-bromo-3-methoxycyclopent-2-enone (1.0 g, 5.23 mmol), 4′-chloro-4-ethylbiphen-3-ylboronic acid (2.03 g, 7.80 mmol) and potassium phosphate (2.23 g, 10.50 mmol) in anhydrous, degassed toluene (25 ml) under an atmosphere of nitrogen is added palladium(II)acetate (24 mg, 0.105 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (86 mg, 0.209 mmol). The reaction is heated at 90° C. for 4 hours and then allowed to cool to room temperature, quenched with water (40 ml) and extracted with ethyl acetate (3×30 ml). The organic extracts are combined, washed with brine (15 ml), dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone (1.29 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530388B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-d3c54b276b0a4d53ae8e78a0751849de |
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| Source note | uspto-grants-2013_09 |
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