関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 4-Iodoanisole | HCID 69676 | — |
| 反応物 | 3-Isopropoxy-4-(tri-n-butylstannyl)-3-cyclobutene-1,2-dione | HCID 2736683 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 3-Isopropoxy-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dione | HCID 14737843 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06462059B1 |
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| 出典データセット | uspto-grants-2002_10 |
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| ORD ID | ord-61e2580eba0e481ab3e0de323c080694 |
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| 出典メモ | uspto-grants-2002_10 |
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