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Di-tert-butyl peroxide → HCID 178445807, Verbindung

HRID 525439
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 525439
C([O:5]OC(C)(C)C)(C)(C)C.[Se](=O)=O.[C:14]([C@H:18]1[CH2:23][CH2:22][C@H:21]([O:24][C:25]2[CH:26]=[C:27]3[C:32](=[CH:33][CH:34]=2)[N:31]=[C:30]([CH3:35])[CH:29]=[CH:28]3)[CH2:20][CH2:19]1)([CH3:17])([CH3:16])[CH3:15]>O1CCOCC1.C(Cl)(Cl)Cl>[C:14]([C@H:18]1[CH2:23][CH2:22][C@H:21]([O:24][C:25]2[CH:26]=[C:27]3[C:32](=[CH:33][CH:34]=2)[N:31]=[C:30]([CH:35]=[O:5])[CH:29]=[CH:28]3)[CH2:20][CH2:19]1)([CH3:17])([CH3:16])[CH3:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 8033Di-tert-butyl peroxideHCID 24007Selenium DioxideHCID 178422868HCID 178422868, Verbindung

Produkt 1

HCID 178445807HCID 178445807, VerbindungAusbeute 20 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6212ChloroformLösungsmittel
HCID 31275
1,4-Dioxane
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

Di-tert-butyl peroxide (1.93 mL, 10.5 mmol) was added to a suspension of selenium dioxide (2.68 g, 24.1 mmol) in 1,4-dioxane (24.00 mL, 307.5 mmol). The mixture was stirred for 30 minutes, then 6-(trans-4-tert-Butyl-cyclohexyloxy)-2-methylquinoline (3.12 g, 10.5 mmol) was added as a solution in 1,4-Dioxane and the mixture was heated overnight at 50° C. The reaction mixture was then cooled to room temperature, diluted in chloroform and filtered through a pad of celite. The filtrate was washed with water. The layers were separated and the combined organic phase was dried over MgSO4, filtered, concentrated under reduced pressure, adsorbed onto silica gel and purified by flash chromatography (0-30% EtOAc in hexanes) to give the title compound as a pale yellow solid in 20% yield. ESI-MS (M+H+): 312.27.

Aufarbeitung

  1. temperatureThe reaction mixture was then cooled to room temperature
  2. filtrationfiltered through a pad of celite
  3. washThe filtrate was washed with water
  4. customThe layers were separated
  5. dry with materialthe combined organic phase was dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. custompurified by flash chromatography (0-30% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-38fa35853a63461985a318089af100a0
Quelldatensatz
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09340527B2

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