Water → Di-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidine-4-yl] Sebacate

HRID 1590926

Reaktionsgleichung

Reaktionsgleichung von HRID 1590926
[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])([CH3:37])C.[OH2:41].[CH2:42]([C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)[CH3:43]>[Mo]=O>[C:1]([O:24][CH:25]1[CH2:30][C:29]([CH3:32])([CH3:31])[N:28]([O:41][CH:42]([CH3:43])[C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[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:39][CH:35]([CH3:38])[C:37]2[CH:5]=[CH:4][CH:3]=[CH:2][CH:1]=2)[C:15]([CH3:21])([CH3:22])[CH2:14]1)=[O:11]

Komponenten

6

Edukt 4

HCID 962WaterHCID 6410tert-Butyl hydroperoxideHCID 7500EthylbenzeneHCID 164282Tinuvin 770

Produkt 1

HCID 19768362Di-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidine-4-yl] SebacateAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 139765Molybdenum oxideKatalysator

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

A mixture of 40.0 g (83 mmol) of di-(2,2,6,6-tetramethylpiperidin-4-yl) sebacate, 2.0 g of molybdenum oxide, and 250 ml of ethylbenzene is heated to 110° C. (nitrogen atmosphere). A commercially available solution of 70% t-butyl hydroperoxide in water (64.3 g, 499 mmol) is added dropwise over 30 min. Water is collected in a Dean-Stark trap. Heating is continued for 90 minutes after the addition. The reaction mixture is filtered and evaporated. The resulting crude oil is dissolved in heptane (300 ml), and this solution is passed through a short column of silica gel. The first 350 ml of filtrate, nearly pure by TLC, is evaporated to give 41.7 g (70% yield) of the title compound, a viscous oil.

Aufarbeitung

  1. customWater is collected in a Dean-Stark trap
  2. temperatureHeating
  3. additionafter the addition
  4. filtrationThe reaction mixture is filtered
  5. customevaporated
  6. dissolutionThe resulting crude oil is dissolved in heptane (300 ml)
  7. customThe first 350 ml of filtrate, nearly pure by TLC, is evaporated

Quellen und Nachweise

ORD-Eintrag
ord-4501b9aa0c7c4d44915ad6a18b89cd8e
Quelldatensatz
uspto-grants-1993_04
Patentnummer
US05204473

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