StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Potassium Hydroxide → 4-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane

HRID 36832
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 36832
[OH-].[K+].OC[C:5]12[CH2:12][O:11][C:8]([CH3:13])([O:9][CH2:10]1)[O:7][CH2:6]2.[CH3:14][O:15]CBr>CS(C)=O.O>[CH3:14][O:15][C:5]12[CH2:6][O:7][C:8]([CH3:13])([O:9][CH2:10]1)[O:11][CH2:12]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 14797Potassium HydroxideHCID 83093Bromomethyl methyl etherHCID 13547990(1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanol

Produkt 1

HCID 199362444-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 679Dimethyl SulfoxideLösungsmittel
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

Powdered potassium hydroxide (16.2 g, 0.290 mol) is suspended in 100 mL of dimethyl sulfoxide and the mixture is stirred at 25° C. for 5 min. Then 4-(hydroxymethyl)-1-methyl-2,6,7-trioxabicyclo[2.2.21octane (10.0 g, 0.062 mol) is added followed by bromomethyl methyl ether (9.3 g, 6.1 mL, 0.074 mol). The reaction mixture is stirred for 30 min and then diluted with water (1 L) and extracted with dichloromethane several times. The combined organic layers are washed with saturated sodium chloride (100 mL), dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 4-(methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane. This crude material is dissolved in methanol (100 mL) and stirred with pyridinium p-toluenesulfonate (1.6 g, 6.200 mmol) in water (100 mL) for 30 min. The pH of the solution is adjusted to 7 with solid sodium bicarbonate and the solvents are removed under reduced pressure. The resulting solids are triturated with methanol and the methanol solution is evaporated to give 2-(methoxymethoxy)-1,1,1-tris(hydroxymethyl)ethane.

Aufarbeitung

  1. stirringThe reaction mixture is stirred for 30 min
  2. extractionextracted with dichloromethane several times
  3. washThe combined organic layers are washed with saturated sodium chloride (100 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a90a004be91b4ef983749cf4eaaa3e0b
Quelldatensatz
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05417959

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion