tert-Butyl hydroperoxide → Tinuvin 123

HRID 1590951

Reaktionsgleichung

Reaktionsgleichung von HRID 1590951
[C:1]([O:5]O)([CH3:4])(C)C.[CH3:7][C:8]1([CH3:40])[CH2:13][CH:12]([O:14][C:15](=[O:37])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]([O:26][CH:27]2[CH2:32][C:31]([CH3:34])([CH3:33])[NH:30][C:29]([CH3:36])([CH3:35])[CH2:28]2)=[O:25])[CH2:11][C:10]([CH3:39])([CH3:38])[NH:9]1>[Mo](=O)(=O)=O.CCCCCCCC>[CH2:15]([O:14][N:30]1[C:29]([CH3:36])([CH3:35])[CH2:28][CH:27]([O:26][C:24](=[O:25])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][C:15]([O:14][CH:12]2[CH2:13][C:8]([CH3:40])([CH3:7])[N:9]([O:5][CH2:1][CH2:4][CH2:8][CH2:13][CH2:12][CH2:11][CH2:10][CH3:38])[C:10]([CH3:39])([CH3:38])[CH2:11]2)=[O:37])[CH2:32][C:31]1([CH3:34])[CH3:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]

Komponenten

5

Edukt 2

HCID 6410tert-Butyl hydroperoxideHCID 164282Tinuvin 770

Produkt 1

HCID 3592789Tinuvin 123Ausbeute 160,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14802Molybdenum trioxideKatalysatorHCID 356OctaneLösungsmittel

Reaktionsbedingungen

Temperatur
115 °C

Versuchsvorschrift

70% Aqueous t-butyl hydroperoxide (140 g, 1.09 mol) is added over a 6 hour period to a mixture of 75.4 g (0.157 mol) of bis(2,2,6,6-tetramethylpiperidin-4-yl)sebacate, 1.25 g (8.7 mmol) of molybdenum trioxide, and 570 ml of n-octane that has been heated to 115° C. under a nitrogen atmosphere. During the addition, the reaction is maintained at reflux. Water is collected in a Dean-Stark trap. Upon completion of the addition, the red reaction mixture is heated at reflux (95°-97° C.) for seven hours to discharge the red color. The molybdenum trioxide is removed by filtration. The yellow filtrate is stirred at ambient temperature for 30 minutes with 15 g of activated charcoal (DARCO) to remove some of the yellow color, and then concentrated at reduced pressure. The crude product is purified by flash chromatography on silica gel (100:3 heptane: ethyl acetate) to afford 92.9 g (80% yield) of the title compound, a colorless oil.

Aufarbeitung

  1. additionDuring the addition
  2. temperaturethe reaction is maintained
  3. temperatureat reflux
  4. customWater is collected in a Dean-Stark trap
  5. additionUpon completion of the addition
  6. customthe red reaction mixture
  7. temperatureis heated
  8. temperatureat reflux (95°-97° C.) for seven hours
  9. customThe molybdenum trioxide is removed by filtration
  10. customto remove some of the yellow color
  11. concentrationconcentrated at reduced pressure
  12. customThe crude product is purified by flash chromatography on silica gel (100:3 heptane: ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-ee9c0c3f01504782a5dadaa0b94f81ca
Quelldatensatz
uspto-grants-1993_04
Patentnummer
US05204473

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