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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031545생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1031545

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물HexafluorobenzeneHCID 9805—
반응물Sodium hydrideHCID 24758—
반응물4-Phenylpiperidin-4-olHCID 96387—
용매DimethylformamideHCID 6228—
생성물4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidineHCID 1464997844%

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04954511
출처 데이터셋uspto-grants-1990_09
ORD IDord-328e9c6847e348d78475cd9183d1ee0d
출처 메모uspto-grants-1990_09