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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133645생성일: 2026년 10월 25일

Hydrogen Peroxide → 1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/133645

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물AcetonitrileHCID 6342—
반응물Boric AcidHCID 7628—
반응물1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
촉매Boric AcidHCID 7628—
용매WaterHCID 962—
용매CyclohexaneHCID 8078—
생성물1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 2337209868%

반응 조건

온도52 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390904B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-3be2a870370043d3af12d94d8a753174
출처 메모uspto-grants-2008_06