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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
Reactant1-Pentanone, 1-[1,1'-biphenyl]-4-yl-HCID 3084882—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product6-[1,1'-Biphenyl]-4-yl-6-butyl-5,6-dihydro-4-hydroxy-2H-pyran-2-oneHCID 54721742—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789440
Source datasetuspto-grants-1998_08
ORD IDord-c6fba34c345347d49ffa28403d506ae5
Source noteuspto-grants-1998_08