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HRID 990761作成日:2026年10月25日

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

https://huagongshe.com/reaction/990761

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Diethyl EtherHCID 3283—
反応物4-IodoanisoleHCID 69676—
反応物3-Isopropoxy-4-(tri-n-butylstannyl)-3-cyclobutene-1,2-dioneHCID 2736683—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-Isopropoxy-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dioneHCID 14737843—

反応条件

温度0 °C

反応手順

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 preci-pitated as a light yellow solid (2.46 g, 54%): 1H NMR (DMSO-d6) δ7.89(d,2H), 7.15(d,2H), 5.45(hept, 1H), 3.82(s,3H), 1.48(d,6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462059B1
出典データセットuspto-grants-2002_10
ORD IDord-61e2580eba0e481ab3e0de323c080694
出典メモuspto-grants-2002_10