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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1590927생성일: 2026년 10월 26일

tert-Butyl hydroperoxide → Di-(1-heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl) Sebacate

https://huagongshe.com/reaction/1590927

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl hydroperoxideHCID 6410—
반응물Tinuvin 770HCID 164282—
촉매Molybdenum trioxideHCID 14802—
용매HeptaneHCID 8900—
생성물Di-(1-heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl) SebacateHCID 5094315872%

반응 조건

온도140 °C

반응 단계

A mixture of 35.0 g (72.8 mmol) of di-(2,2,6,6-tetramethylpiperidin-4-yl) sebacate, 58.3 (582 mmol) of 90% aqueous t-butyl hydroperoxide, 2.0 g of molybdenum trioxide, and 250 ml of heptane is heated at 140° C. in a Fischer-Porter bottle. The pressure is maintained at 40-50 psi by occasional venting. Heating is discontinued after 7 hours. An additional portion (20.0 g) of 90% t-butyl hydroperoxide is added and the reaction mixture is heated for one hour at 140° C. The reaction is nearly colorless by this time. The reaction mixture is cooled and filtered to remove the catalyst. The organic phase is separated, dried over magnesium sulfate, and concentrated to 100 ml total volume. This solution is passed through silica gel with heptane as the eluent. The filtrate is evaporated to yield 36.9 g (72% yield) of the title compound, a nearly colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05204473
출처 데이터셋uspto-grants-1993_04
ORD IDord-b4149a4b889d4dcfafbfd69d2eba3c37
출처 메모uspto-grants-1993_04