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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2083671생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2083671

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 22457766.6%

반응 단계

1.96 Parts piperidine, 1.91 parts potassium iodide and 25 parts deionized water are combined and gently heated under a nitrogen atmosphere. To this slurry is then added 2.75 parts of potassium bicarbonate, followed by 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, washed with water and saturated sodium chloride solution, 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 66.6% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04086234
출처 데이터셋uspto-grants-1978_04
ORD IDord-ac663a5a1f92405a993d0944f95d3bf9
출처 메모uspto-grants-1978_04