HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254235Generated: October 31, 2026
Ethyl 2-oxovalerate → 4-HYDROXY-4-METHYL-5-HEXENOIC ACID gamma LACTONE
https://huagongshe.com/reaction/254235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-oxovalerate | HCID 123521 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-HYDROXY-4-METHYL-5-HEXENOIC ACID gamma LACTONE | HCID 102550 | 53.6% |
Reaction Steps
To a solution of ethyl 2-ketopentanoate (10 mL, 71 mmol) in 100 mL of THF at −78° C. was added dropwise a solution of 1.0 M vinyl magnesium bromide (80 mL, 80 mmol). After completion of the addition, the mixture was stirred for two more hours, the cooling bath was removed and the mixture was gradually warmed to ambient temperature. After the removal of the most of the solvent, the residue was poured to 2N HCl aqueous solution, extracted with ethyl acetate and dried over MgSO4. Purification by lash column chromatography on silica gel with DCM as elute afforded 4.80 grams of 5-methyl-5-vinyl-dihydro-furan-2-one. 1H-NMR (300 MHz, CDCl3) δ (ppm): 5.824-5.917 (dd, 1H); 5.29 (d, 1H); 5.13 (d, 1H); 2.50-2.56 m, (2H); 2.07-2.18 (m, 2H); 1.48 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875607B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-bf75d2d060164d01b7d93ce6a7fb772f |
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| Source note | uspto-grants-2011_01 |
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