HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407843Generated: October 30, 2026
Acetone → 5-(2,4,6-Trimethylphenyl)-4-hydroxycyclopent-2-enone
https://huagongshe.com/reaction/407843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | (2,4,6-Trimethylphenyl)furan-2-ylmethanol | HCID 49962474 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2,4,6-Trimethylphenyl)-4-hydroxycyclopent-2-enone | HCID 66684008 | — |
Reaction Steps
A solution of (2,4,6-trimethylphenyl)furan-2-ylmethanol (27.8 g, 129 mmol) in acetone (730 ml) and water (100 ml) is heated to 55° C. and polyphosphoric acid (2 g) is added. The mixture is stirred at 55° C. for 7 hours, then cooled to room temperature overnight. The reaction mixture is concentrated under reduced pressure to remove most of the acetone then ethyl acetate (500 ml) is added, and the reaction mixture is partitioned. The aqueous phase is extracted into ethyl acetate and the organic solutions are combined, washed with saturated aqueous sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give 5-(2,4,6-trimethylphenyl)-4-hydroxycyclopent-2-enone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754242B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-03a80a937a0041a3a44d7c9afb53b33b |
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| Source note | uspto-grants-2014_06 |
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