Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 1,2-Phenanthrenedione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 반응물 | 9,10-Bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthrene | HCID 68551787 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1,2-Phenanthrenedione | HCID 3080566 | 76% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08338027B2 |
| 출처 데이터셋 | uspto-grants-2012_12 |
| ORD ID | ord-9ca737a9f5214428ab90c08d96b3b452 |
| 출처 메모 | uspto-grants-2012_12 |