HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481850Generated: October 26, 2026
Methyl acetoacetate → 6-Butyl-5,6-dihydro-4-hydroxy-6-phenyl-2H-pyran-2-one
https://huagongshe.com/reaction/481850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Valerophenone | HCID 66093 | — |
| Product | 6-Butyl-5,6-dihydro-4-hydroxy-6-phenyl-2H-pyran-2-one | HCID 54699368 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 2.7 mL of methyl acetoacetate, 1.1 g of NaH 60% dispersion in oil, 12.5 mL of 2.0M n-butyl lithium in hexane, 5.1 mL of valerophenone and 125 mL of tetrahydrofuran. After addition of the ketone, the reaction was stirred for 10 minutes at 0° C. then allowed to warm to room temperature overnight. The crude product was triturated from diethyl ether to afford a solid (m.p. 124°-126° C.). 1H NMR (CDCl3) δ0.85 (t, 3H), 1.28 (m, 4H), 1.97 (m, 2H), 2.90 (dd, 2H), 3.30 (dd, 2H), 7.28-7.42 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789440 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-29591afed28d4ec5b33077c43e89ffc6 |
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| Source note | uspto-grants-1998_08 |
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