HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193026Generated: November 3, 2026
Acetone → 5-(4-Bromo-2,6-dimethylphenyl)-4-hydroxycyclopent-2-enone
https://huagongshe.com/reaction/1193026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol | HCID 66709611 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-Bromo-2,6-dimethylphenyl)-4-hydroxycyclopent-2-enone | HCID 58070855 | — |
Reaction Steps
Polyphosphoric acid (500 mg) is added to a warm (55° C.) solution of ([4-bromo-2,6-dimethylphenyl]furan-2-yl)methanol (843 mg, 3 mmol) in acetone (8 ml) and water (2 ml) and the mixture is heated at 55° C. for 24 hours. The mixture is cooled to room temperature and the acetone is removed under reduced pressure. The remaining mixture is partitioned between diethyl ether (20 ml) and water (20 ml). The aqueous phase is extracted with ether (2×50 ml), and then the organic phases are combined, washed with saturated aqueous sodium bicarbonate solution (20 ml), and brine (20 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 5-(4-bromo-2,6-dimethylphenyl)-4-hydroxycyclopent-2-enone (596 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680339B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-8abbc7d961744bd688b50bda39744e23 |
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| Source note | uspto-grants-2014_03 |
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