참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 반응물 | 2,2,6,6-Tetramethyl-4-piperidyl benzoate | HCID 579967 | — |
| 촉매 | Molybdenum trioxide | HCID 14802 | — |
| 용매 | Octane | HCID 356 | — |
| 생성물 | 4-Benzoyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidine | HCID 15169994 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05021577 |
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| 출처 데이터셋 | uspto-grants-1991_06 |
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| ORD ID | ord-3fb9a37cc3b047c498cccbbc2b2d7b7b |
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| 출처 메모 | uspto-grants-1991_06 |
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