戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1489552作成日:2026年10月25日

Toluene → 7-Phenyl-1-tetralone

https://huagongshe.com/reaction/1489552

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物Phenyl dihydrogen orthoborateHCID 78412—
反応物5,6,7,8-Tetrahydro-8-oxo-2-naphthalenyl 1,1,1-trifluoromethanesulfonateHCID 11000871—
溶媒WaterHCID 962—
生成物7-Phenyl-1-tetraloneHCID 377823582.4%

反応条件

温度90 °C

反応手順

While stirring a mixture comprising 15.32 g (52.06 mmol) of 7-trifluoromethanesulfonyloxy-3,4-dihydro-1(2H)-naphthalenone obtained in the Synthesis Example A-1, 12.7 g (104.12 mmol) of phenylboric acid, 10.8 g (78.09 mmol) of potassium carbonate and 450 ml of toluene at room temperature, nitrogen gas was bubbled thereinto for 30 minutes. Next, 1.81 g (1.57 mmol) of tetrakistriphenylphosphine palladium was added thereto. The mixture was slowly heated to thereby maintain the bulk temperature at about 90° C. After stirring at this temperature for 90 minutes, the reaction mixture was cooled and water was added thereto. The insoluble matters were filtered through celite and thoroughly washed with ethyl acetate. The organic phase was collected, washed successively with a saturated aqueous solution of sodium hydrogencarbonate, water, 1N hydrochloric acid, water and a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was subjected to silica gel column chromatography. After successively eluting with hexane:ethyl acetate in a ratio ranging from 20:1 (v/v) to 12:1 (v/v), 9.53 g of the title compound was obtained as white crystals. Yield 82%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05679671
出典データセットuspto-grants-1997_10
ORD IDord-dc828b2e6d30423fa28d3dafcaa74500
出典メモuspto-grants-1997_10