戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2195577作成日:2026年10月27日

Tetrahydrofuran → 1,2-Phenanthrenedione

https://huagongshe.com/reaction/2195577

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物9,10-Bis(t-butyldimethylsilyloxy)-2-iodo-9,10-dihydro-phenanthreneHCID 68551787—
溶媒EthanolHCID 702—
生成物1,2-PhenanthrenedioneHCID 308056676%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08338027B2
出典データセットuspto-grants-2012_12
ORD IDord-9ca737a9f5214428ab90c08d96b3b452
出典メモuspto-grants-2012_12