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HRID 616577생성일: 2026년 10월 26일

Potassium Chloride → (E)-1-tert-Butyl-2-[1-(tert-butylperoxy)cyclohexyl]diazene

https://huagongshe.com/reaction/616577

반응식

참여 물질

역할이름HCID투입량
반응물Potassium ChlorideHCID 4873—
반응물tert-Butyl hydroperoxideHCID 6410—
반응물Potassium HydroxideHCID 14797—
반응물Sodium HydroxideHCID 14798—
반응물1-t-Butylazo-1-chlorocyclohexaneHCID 23344784—
용매WaterHCID 962—
생성물(E)-1-tert-Butyl-2-[1-(tert-butylperoxy)cyclohexyl]diazeneHCID 2334475388%

반응 조건

온도20 °C

반응 단계

To a solution of 42 grams (0.64 moles) of 85% potassium hydroxide in 100 ml. of water, cooled to 15° C in a 2 liter jacketed reactor was added 81 grams (0.81 moles) of 90% t-butylhydroperoxide slowly and with rapid stirring. The temperature was held at 20°-25° C by the rate of addition and by circulating 15° C water through the reactor jacket. After the addition was complete, the reaction was stirred for 30 minutes at 20° C and then 118 grams (0.58 moles) of 1-t-butylazo-1-chlorocyclohexane was added dropwise over a 30 minute period holding the temperature at 20°-22° C. After the addition was complete the reaction was stirred for 15 minutes at 20° C. It was then cooled to 0°-5° C and stirred for 90 minutes. A 0.2 mole (16 grams) portion of 50% NaOH was then added and the reaction stirred for 15 minutes. Ice water was then added until the potassium chloride dissolved. The mixture was extracted with 200ml. of pentane, the pentane extract washed with ice cold water saturated NaHCO3 solution, dried over anhydrous sodium sulfate, filtered and the pentane evaporated under reduced pressure at 10° C to leave 130 grams (88% yield) of crude 1-t-butylazo-1-(t-butylperoxy)-cyclohexane. The product was stored in a dry ice chest.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04075199
출처 데이터셋uspto-grants-1978_02
ORD IDord-c1dec79f87ca48f2bd04771c6a43c499
출처 메모uspto-grants-1978_02