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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52388생성일: 2026년 10월 26일

Water → 1-Cyclohexyloxy-2,2,6,6-tetramethyl-4-acetoxypiperidine

https://huagongshe.com/reaction/52388

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물CyclohexaneHCID 8078—
반응물4-Acetoxy-2,2,6,6-tetramethylpiperidineHCID 14149715—
촉매Molybdenum oxideHCID 139765—
생성물1-Cyclohexyloxy-2,2,6,6-tetramethyl-4-acetoxypiperidineHCID 19698886—

반응 조건

온도25 °C

반응 단계

60 g (301 mmol) of 4-acetoxy-2,2,6,6-tetramethylpiperidine are dissolved in 300 ml of cyclohexane under nitrogen in a 1.5 l sulfonation flask fitted with magnetic stirrer, water separator, thermometer and dropping funnel. 4.3 g (30 mmol) of molybdenum oxide are added. 154 g (1.2 mol) of an aqueous 70% solution of t-butyl hydroperoxide are extracted three times with 35 ml of cyclohexane in each case, and the organic phase is dried over sodium sulfate and transferred into the dropping funnel. The reaction mixture is warmed to reflux, and the t-butyl hydroperoxide solution is added dropwise over the course of 2 hours. After a further 2 hours, the elimination of water is complete. The mixture is held at the reflux temperature overnight and is then cooled to 25° C., and the catalyst is filtered off. Ice is added, a little sodium sulfite is added in order to destroy the excess hydroperoxide, and the organic phase is then separated off, washed with water and dried over sodium sulfate, and the solvent is removed on a Rotavap.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616637
출처 데이터셋uspto-grants-1997_04
ORD IDord-794b65abecf44a6db554c7d58fadf8bc
출처 메모uspto-grants-1997_04