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HRID 1650040생성일: 2026년 10월 27일

Sodium Chloride → Di-(1-nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) Sebacate

https://huagongshe.com/reaction/1650040

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물tert-Butyl hydroperoxideHCID 6410—
반응물Tinuvin 770HCID 164282—
촉매Titanium tetrabutoxideHCID 21801—
용매NonaneHCID 8141—
생성물Di-(1-nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) SebacateHCID 538868026%

반응 조건

온도151 °C

반응 단계

A 2-phase mixture of 85.7 g (0.666 mol) of 70% aqueous tert-butyl hydroperoxide, 200 ml of n-nonane and 15 g of sodium chloride is agitated in a separatory funnel. The organic layer is dried over anhydrous magnesium sulfate. A mixture of 40.0 g (0.0832 mol) of bis-(2,2,6,6-tetramethylpiperidin-4-yl) sebacate and the tert-butyl hydroperoxidenonane solution is heated to reflux (151° C.) under a nitrogen atmosphere. To this mixture is added over a 10-minute period, a solution of 5.0 g of titanium tetrabutoxide in 50 ml of nonane. The reaction mixture turns red. Water is collected in a Dean Stark trap. The reaction mixture is heated at reflux for 17 hours. Another 5.0 g of titanium tetrabutoxide is added, and the reaction mixture is heated at reflux for an additional 7 hours. Solids are removed by filtration, and the filtrate is concentrated under reduced pressure. The crude red oil obtained is purified by chromatography (Waters Prep 500A HPLC; 29:1 heptane:ethyl acetate) to give 3.6 g (6% yield) or the title compound as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04921962
출처 데이터셋uspto-grants-1990_05
ORD IDord-ced0d83a439f497ab88409c2f77ac965
출처 메모uspto-grants-1990_05