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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2072814생성일: 2026년 10월 27일

Water → 4-(4-Methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/2072814

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물HexafluorobenzeneHCID 9805—
반응물Sodium hydrideHCID 24758—
반응물1-Methyl-4-(4-methylphenyl)piperidin-4-OLHCID 14837037—
용매DimethylformamideHCID 6228—
생성물4-(4-Methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 14837063—

반응 조건

온도85 °C

반응 단계

To a suspension of sodium hydride (2.2 g, 60% in oil) in 20 ml of dimethylformamide, was added a solution of 11.0 g of 4-hydroxy-4-(4-methylphenyl)-1-methylpiperidine in 50 ml of dimethylformamide. After heating to 85° C. for thirty minutes, the mixture was cooled with an ice-bath, and treated over a period of ten minutes with a solution of 7 ml of hexafluorobenzene in 20 ml of dimethylformamide. After stirring at ambient temperature for twenty hours, the mixture was poured into 200 ml water, stirred for five minutes, then extracted with ethyl acetate (2×). The organic layer was washed with water (2×), followed by a saturated solution of sodium chloride, and dried over anhydrous magnesium sulfate. After filtering, evaporation of the solvent afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 10% methanol/dichlormethane). The desired fractions were combined, and evaporated to yield 13 g of (4-(4-methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy) piperidine as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04914204
출처 데이터셋uspto-grants-1990_04
ORD IDord-b02a2d5f4e6740f49d43218d4745d124
출처 메모uspto-grants-1990_04