Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322802생성일: 2026년 10월 24일
1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → 1-(Cyclooct-2-enyloxy)-2,2,6,6-tetramethyl-4-hydroxypiperidine
https://huagongshe.com/ko/reaction/322802
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine | HCID 5395 | — |
| 반응물 | 1-Cyclooctene | HCID 13609 | — |
| 생성물 | 1-(Cyclooct-2-enyloxy)-2,2,6,6-tetramethyl-4-hydroxypiperidine | HCID 69905305 | 36% |
반응 단계
A mixture of 15.0 g (0.09 mol) of 1-oxyl-4-hydroxy-2,2,6,6-tetramethylpiperidine and 126.6 g (1.15 mol) of cyclooctene is heated under a nitrogen atmosphere at 87-88° C. for 40 hours. The reaction mixture is filtered to remove 1,4-dihydroxy-2,2,6,6-tetramethylpiperidine, and the filtrate is washed with 5% ascorbic acid (2×50 mL) and distilled water (2×50 mL). The organic phase is dried over anhydrous magnesium sulfate and the volatiles removed in vacuo. The residue is crystallized from heptane to give 4.40 g (36% yield) of the title compound as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06211378B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-0ca62645de064477b93f5fe01b344fe4 |
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| 출처 메모 | uspto-grants-2001_04 |
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