Triphenylphosphine → Phosphonium, [3-(methoxymethoxy)propyl]triphenyl-, bromide

HRID 493902

Reaktionsgleichung

Reaktionsgleichung von HRID 493902
[Br:1][CH2:2][CH2:3][CH2:4][O:5][CH2:6][O:7][CH3:8].[C:9]1([P:15]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C1(C)C=CC=CC=1>[Br-:1].[CH3:8][O:7][CH2:6][O:5][CH2:4][CH2:3][CH2:2][P+:15]([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1

Komponenten

4

Edukt 2

HCID 11776TriphenylphosphineHCID 127092881-Bromo-3-methoxymethoxypropane

Produkt 1

HCID 11178287Phosphonium, [3-(methoxymethoxy)propyl]triphenyl-, bromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a solution of 1-bromo-3-(methoxymethoxy)propane (0.46 g, 2.5 mmol) in anhydrous toluene (1.5 mL) was added triphenylphoshine (0.71 g, 2.7 mmol) under argon with stirring. The mixture was heated at 100° C. for 20 h and cooled to room temperature. The liquid was decanted and the solid residue was grounded with spatula, filtered and washed several times with ether. After drying overnight in vacuum dessicator colorless crystals of phosphonium salt A (0.98 g, 88%) could be used in the Wittig reaction without further purification.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. customThe liquid was decanted
  3. filtrationfiltered
  4. washwashed several times with ether
  5. dry with materialAfter drying overnight in vacuum dessicator colorless crystals of phosphonium salt A (0.98 g, 88%)
  6. customcould be used in the Wittig reaction without further purification

Quellen und Nachweise

ORD-Eintrag
ord-1099846e47874159896379355ca06fd9
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07538098B2

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