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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2083670생성일: 2026년 10월 26일

Potassium Iodide → 2,2-Diphenyl-4-piperidin-1-ylbutanenitrile

https://huagongshe.com/reaction/2083670

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물PiperidineHCID 8082—
반응물Potassium HydroxideHCID 14797—
반응물4-Bromo-2,2-diphenylbutyronitrileHCID 96575—
용매WaterHCID 962—
생성물2,2-Diphenyl-4-piperidin-1-ylbutanenitrileHCID 22457786.1%

반응 단계

To 1.96 parts of piperidine is added 1.91 parts of potassium iodide and 25 parts deionized water under a nitrogen atmosphere. The mixture is gently warmed and 1.65 parts of potassium hydroxide and 7.51 parts of 2,2-diphenyl-4-bromobutyronitrile are added. The temperature is raised to reflux and maintained thereat for 4.5 hours. After cooling to room temperature, the reaction mixture is extracted three times with 14 part portions of ethyl ether. The ether extracts are combined, and extracted four times with 25 parts by volume portions of a dilute acetic acid solution. The acid extracts are combined, neutralized to about pH 10 with 50% sodium hydroxide solution, and extracted again with ethyl ether. The ether extracts are combined, washed twice with 50 parts by volume portions of a saturated sodium chloride solution, and dried over anhydrous potassium carbonate. The solvent is removed under reduced pressure to afford, as an off-white solid, in 86.1% yield, 2,2-diphenyl-4-piperidinobutyronitrile. This compound melts at 74° - 77° C., and is represented by the following structural formula. ##STR16##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04086234
출처 데이터셋uspto-grants-1978_04
ORD IDord-d64643250fdf4ac4984ab2f06ad440e5
출처 메모uspto-grants-1978_04