참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Boric Acid | HCID 7628 | — |
| 반응물 | 1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine | HCID 688178 | — |
| 촉매 | Boric Acid | HCID 7628 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine | HCID 23372098 | 68% |
반응 단계
A solution of 0.100 g (0.360 mmol) of ferrous sulfate heptahydrate and 0.112 g (1.82 mmol) of boric acid in 4 ml of water is added to a mixture of 5.00 g (18.1 mmol) of 1-oxyl-4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 27 ml of acetonitrile, and 19 ml of cyclohexane. The mixture is heated to 52° C. A solution of 4.98 g (73 mmol) of 50% aqueous hydrogen peroxide is added dropwise over 2.75 hours to the reaction mixture while the temperature is brought to and maintained at reflux (63° C.). A solution of 0.051 g of ferrous sulfate heptahydrate and 0.042 g of boric acid in 2 ml of water is added to the reaction mixture 1.25 hours after the peroxide addition is started. After the peroxide is added, the reaction mixture is heated at reflux for 30 minutes, then allowed to cool slowly. Work-up and purification according to the procedure of Example 5 afford 4.42 g (68% yield) of the title compound, a colorless syrup, GC assay 99.3%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390904B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-3be2a870370043d3af12d94d8a753174 |
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| 출처 메모 | uspto-grants-2008_06 |
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