HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481844Generated: October 30, 2026
Ethyl Acetoacetate → 6-[1,1'-Biphenyl]-4-yl-6-butyl-5,6-dihydro-4-hydroxy-2H-pyran-2-one
https://huagongshe.com/reaction/481844
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Pentanone, 1-[1,1'-biphenyl]-4-yl- | HCID 3084882 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6-[1,1'-Biphenyl]-4-yl-6-butyl-5,6-dihydro-4-hydroxy-2H-pyran-2-one | HCID 54721742 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 13 g ethyl acetoacetate, 5.3 g of NaH 60% dispersion in oil, 60 mL of 1.6M n-butyl lithium in hexane, 21 g of 1-[1,1'-biphenyl]-4-yl-1-pentanone and 300 mL of tetrahydrofuran. After addition of the ketone, the reaction was stirred 15 minutes at -78° C. and 2 hours at room temperature. The crude reaction mixture afforded a solid which was washed with CH2 Cl2 and two times with ethyl acetate (m.p. 165°-170° C.). 'H NMR(d6 -DMSO) δ0.7-1.9 (m, 7H), 2.0 (m, 2H), 3.0 (s, 2H), 4.9 (s, 1H), 7.3-7.8 (m, 9H), 11.3 (s, 1H).
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-c6fba34c345347d49ffa28403d506ae5 |
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| Source note | uspto-grants-1998_08 |
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