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HRID 843035생성일: 2026년 10월 25일

Methane → 3-Isopropoxy-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/843035

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Diethyl EtherHCID 3283—
반응물4-IodoanisoleHCID 69676—
반응물3-Isopropoxy-4-(tri-n-butylstannyl)-3-cyclobutene-1,2-dioneHCID 2736683—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-Isopropoxy-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dioneHCID 14737843—

반응 조건

온도0 °C

반응 단계

To a solution of 3-isopropoxy-4-(tri-n-butyl-stannyl)-3-cyclobutene-1,2-dione (J. Org. Chem. 1990, 55, 5359-5364) (8.00 g, 18.65 mmol) in N,N-dimethyl-formamide (40 mL) was added 4-iodoanisole (4.85 g, 20.72 mmol). The flask was purged with nitrogen and cooled to 0° C. Benzylchloro-bis-(triphenylphosphine)palladium (II) (0.942 g, 1.24 mmol) and cuprous iodide (0.355 g, 1.87 mmol) were added and the mixture was stirred at room temperature overnight. Diethylether (200 mL) was added and the mixture was washed successively with saturated aqueous ammonium chloride, 10% aqueous potassium fluoride and saturated brine. The organic phase was filtered through a plug of silica. The filtrate was dried (MgSO4) and concentrated to give crude product which was dissolved in hot ethyl acetate, decolorized (charcoal) and filtered. The filtrate was treated with hexane and allowed to cool. 3-Isopropoxy-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dione precipitated as a light yellow solid (2.46 g, 54%): 1H NMR (DMSO-d6) δ 7.89(d,2H), 7.15(d,2H), 5.45(hept,1H), 3.82(s,3H), 1.48(d,6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06376555B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-60165b8f3d994835aa5470d7b3a96c22
출처 메모uspto-grants-2002_04