HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1590950Erstellt: 25. Oktober 2026
Water → Bis(1-cyclooctyloxy-2,2,6,6-tetramethylpiperidin-4-yl)sebacate
https://huagongshe.com/reaction/1590950
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | tert-Butyl hydroperoxide | HCID 6410 | — |
| Edukt | Cyclooctane | HCID 9266 | — |
| Edukt | Tinuvin 770 | HCID 164282 | — |
| Katalysator | Molybdenum trioxide | HCID 14802 | — |
| Produkt | Bis(1-cyclooctyloxy-2,2,6,6-tetramethylpiperidin-4-yl)sebacate | HCID 19768323 | 68% |
Reaktionsschritte
A mixture of 75 g (156 mmol) of bis(2,2,6,6-tetramethylpiperidin-4-yl)sebacate, 1.3 g of molybdenum trioxide, and 475 ml of cyclooctane is heated to 118° C. To this mixture is added 130 g (1.01 mol) of 70% aq. t-butyl hydroperoxide during a 5 hour period. The reaction mixture is maintained at reflux during the addition, and water is collected in a Dean-Stark trap. The red reaction mixture is heated for 7 hours after the addition to discharge the red color. Solids are removed by filtration, and the filtrate is evaporated to give a yellow oil. Purification (Waters Prep. 500 A HPLC, 20:1 hexane: ethyl acetate) affords 78.7 g (68%) of the title compound, a colorless syrup.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05204473 |
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| Quelldatensatz | uspto-grants-1993_04 |
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| ORD ID | ord-135339ad1ec14beebaec2bacd700cfd8 |
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| Quellennotiz | uspto-grants-1993_04 |
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