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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2195577생성일: 2026년 10월 26일

Tetrahydrofuran → 1,2-Phenanthrenedione

https://huagongshe.com/reaction/2195577

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물9,10-Bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthreneHCID 68551787—
용매EthanolHCID 702—
생성물1,2-PhenanthrenedioneHCID 308056676%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338027B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-9ca737a9f5214428ab90c08d96b3b452
출처 메모uspto-grants-2012_12