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Tetrahydrofuran → 1,2-Phenanthrenedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | 9,10-Bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthrene | HCID 68551787 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1,2-Phenanthrenedione | HCID 3080566 | 76% |
反応手順
Into a 20 mL volume eggplant-shaped flask, 80 mg of the above-prepared 9,10-bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthrene dimer, 10 mL of tetrahydrofuran, 43 mg of ethanol, and 0.4 mL of tetrabutylammonium fluoride were added and stirred at room temperature in air. The resultant reaction mixture was allowed to stand. Thereafter, the precipitate was collected by filtration and washed, thereby to give 28 mg of a phenanthrenequinone compound represented by the following chemical structural formula (1b-1) (hereinafter referred to as a “phenanthrenequinone compound (1b-1)”) (yield 76%) as a reddish brown-colored solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08338027B2 |
| 出典データセット | uspto-grants-2012_12 |
| ORD ID | ord-9ca737a9f5214428ab90c08d96b3b452 |
| 出典メモ | uspto-grants-2012_12 |