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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2083672생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2083672

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물PiperidineHCID 8082—
반응물4-Bromo-2,2-diphenylbutyronitrileHCID 96575—
반응물Potassium BicarbonateHCID 516893—
용매WaterHCID 962—
생성물2,2-Diphenyl-4-piperidin-1-ylbutanenitrileHCID 22457775.3%

반응 단계

To a warmed mixture of 1.96 parts piperidine, 1.91 parts potassium iodide and 25 parts deionized water under a nitrogen atmosphere is added 3.46 parts potassium bicarbonate and 7.51 parts of 2,2-diphenyl-4-bromobutyronitrile. The mixture is heated 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 six times with 25 parts by volume portions of dilute acetic acid solution. The acid extracts are combined, basified to about pH 10 - 12 with 50% sodium hydroxide solution, and again extracted with ethyl ether. The ether extracts are combined and dried over anhydrous potassium carbonate. Removal of the solvent affords 2,2-diphenyl-4-piperidinobutyronitrile, identical to the product of Example 22, in a 75.3% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04086234
출처 데이터셋uspto-grants-1978_04
ORD IDord-f0824a4fd71640d1b36e68157487fe77
출처 메모uspto-grants-1978_04