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

HRID 1590927

Reaktionsgleichung

Reaktionsgleichung von HRID 1590927
[C:1]([O:24][CH:25]1[CH2:30][C:29]([CH3:32])([CH3:31])[NH:28][C:27]([CH3:34])([CH3:33])[CH2:26]1)(=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH:13]1[CH2:18][C:17]([CH3:20])([CH3:19])[NH:16][C:15]([CH3:22])([CH3:21])[CH2:14]1)=[O:11].[C:35]([O:39]O)([CH3:38])(C)C>[Mo](=O)(=O)=O.CCCCCCC>[C:1]([O:24][CH:25]1[CH2:30][C:29]([CH3:32])([CH3:31])[N:28]([O:39][CH2:35][CH2:38][CH2:17][CH2:18][CH2:13][CH2:14][CH3:15])[C:27]([CH3:34])([CH3:33])[CH2:26]1)(=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH:13]1[CH2:18][C:17]([CH3:19])([CH3:20])[N:16]([O:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH3:4])[C:15]([CH3:21])([CH3:22])[CH2:14]1)=[O:11]

Komponenten

5

Edukt 2

HCID 6410tert-Butyl hydroperoxide2×HCID 164282Tinuvin 770

Produkt 1

HCID 50943158Di-(1-heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl) SebacateAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14802Molybdenum trioxideKatalysatorHCID 8900HeptaneLösungsmittel

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. temperatureThe pressure is maintained at 40-50 psi by occasional venting
  2. temperatureHeating
  3. temperaturethe reaction mixture is heated for one hour at 140° C
  4. temperatureThe reaction mixture is cooled
  5. filtrationfiltered
  6. customto remove the catalyst
  7. customThe organic phase is separated
  8. dry with materialdried over magnesium sulfate
  9. concentrationconcentrated to 100 ml total volume
  10. customThe filtrate is evaporated

Quellen und Nachweise

ORD-Eintrag
ord-b4149a4b889d4dcfafbfd69d2eba3c37
Quelldatensatz
uspto-grants-1993_04
Patentnummer
US05204473

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