HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501784Generated: November 1, 2026
Potassium Hydroxide → 2(5H)-Furanone, 4-hydroxy-3,5-dimethyl-
https://huagongshe.com/reaction/1501784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-bromo-2-methyl-3-oxopentanoate | HCID 15758245 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2(5H)-Furanone, 4-hydroxy-3,5-dimethyl- | HCID 54698897 | — |
Reaction Steps
To ethyl 4-bromo-2-methyl-3-oxopentanoate (7.49 g, 31.6 mmol) was added cold potassium hydroxide (4.7 g, 84 mmol) in water (36 mL) at 0° C., the resulting mixture was vigorously stirred at 0° C. for 4 h. The reaction mixture was extracted with methylene chloride (2×100 mL), the alkaline phase was acidified to ph 1 by 6N hydrogen chloride followed by extraction with methylene chloride (3 times 100 mL). The combined latter organic phase was dried over sodium sulfate, and concentrated to give 4-hydroxy-3,5-dimethylfuran-2(5H)-one. LCMS: (M+23)+: 151.10, 1HNMR (500 MHz, CDCl3), δ4.882-4.842 (dd, J=6.8 Hz, 1H), 3.744 (s, 1H), 1.759(s, 3H). 1.526-1.513 (d, J=6.8 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206198B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-df09342a9f8f48cd82a8f2a953f6a19b |
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| Source note | uspto-grants-2015_12 |
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