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HRID 1031545作成日:2026年10月26日

Water → 4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidine

https://huagongshe.com/reaction/1031545

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物HexafluorobenzeneHCID 9805—
反応物Sodium hydrideHCID 24758—
反応物4-Phenylpiperidin-4-olHCID 96387—
溶媒DimethylformamideHCID 6228—
生成物4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidineHCID 1464997844%

反応条件

温度50 °C

反応手順

To a suspension of sodium hydride (60% in oil, 6.4 g) in 50 ml of dry dimethylformamide was added, over a period of ten minutes, a solution of 25 g of 4-hydroxy-4-phenylpiperidine in 100 ml of dry dimethylformamide. After stirring at 50° C., for thirty minutes, the reaction mixture was cooled to ice bath temperature (5° C.). A solution of 18.6 ml of hexafluorobenzene in 100 ml of dry dimethylformamide was then added over a period of thirty minutes, and the resulting mixture stirred at ambient temperature for twenty hours. The mixture was poured into 500 ml water, stirred for five minutes, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, evaporation of the solvents afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 20% methanol/dichloromethane) to afford 21 g (44%) of 4-(2,3,4,5,6-pentafluorophenoxy)-4-phenylpiperidine as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04954511
出典データセットuspto-grants-1990_09
ORD IDord-328e9c6847e348d78475cd9183d1ee0d
出典メモuspto-grants-1990_09