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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1493525생성일: 2026년 10월 26일

tert-Butyl hydroperoxide → 4-Benzoyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/1493525

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl hydroperoxideHCID 6410—
반응물2,2,6,6-Tetramethyl-4-piperidyl benzoateHCID 579967—
촉매Molybdenum trioxideHCID 14802—
용매OctaneHCID 356—
생성물4-Benzoyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidineHCID 15169994—

반응 조건

온도120 °C

반응 단계

A mixture of 55.3 grams (0.2 mol) of 4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 2.8 grams of molybdenum trioxide and 250 ml of n-octane is heated to 120° C. A solution of 90.2 grams (0.7 mol) of 70% aqueous tert-butyl hydroperoxide is added dropwise to the hot reaction mixture. Water is removed by azeotropic distillation and collected in a Dean-Stark trap. The reaction mixture is heated at reflux till the red color of the intermediate N-oxyl compound disappears. Solids are removed by filtration, and the filtrate is concentrated under vacuum to give an oil. Purification of the oil by flash chromatography on silica gel (100:3 heptane: ethyl acetate) affords 4-benzoyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidine as a mixture of octyloxy isomers. Further elution of the chromatographic column with 50:3 heptane:ethyl acetate affords the title compound as a mixture of octanediyl isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05021577
출처 데이터셋uspto-grants-1991_06
ORD IDord-3fb9a37cc3b047c498cccbbc2b2d7b7b
출처 메모uspto-grants-1991_06