Reaktion #52686

Reaktionsgleichung

diethylazodicarboxylate

Triphenylphosphine

3-tert-butyl-4-hydroxybenzaldehyde

2-hydroxyethylmorpholine

→

3-tert-butyl-4-(2-morpholin-4-ylethoxy)benzaldehyde

Ausbeute 44.0%

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction was concentrated under reduced pressure
2. 2
   Sonstigepartitioned between 2N hydrochloric acid (200 ml) and ethyl acetate (150 ml)
3. 3
   ExtraktionThe aqueous layer was extracted with ethyl acetate (2×150 ml)
4. 4
   Extraktionextracted with ethyl acetate (3×150 ml)
5. 5
   TrocknenThe combined organic layers were dried over magnesium sulfate
6. 6
   Einengenconcentrated

Vorschrift

Triphenylphosphine (5.89 g, 22.44 mmol) was added to a solution of 3-tert-butyl-4-hydroxybenzaldehyde (4 g, 22.44 mmol) in tetrahydrofuran (40 ml), followed by addition of 2-hydroxyethylmorpholine (2.94 g, 22.44 mmol) and then the dropwise addition of diethylazodicarboxylate (3.91 g, 22.44 mmol). The mixture was allowed to stir at room temperature for 3 days. The reaction was concentrated under reduced pressure and partitioned between 2N hydrochloric acid (200 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (2×150 ml), basified to pH 9 with solid sodium bicarbonate, saturated with solid sodium chloride and extracted with ethyl acetate (3×150 ml). The combined organic layers were dried over magnesium sulfate and concentrated to afford 2.8 g (44%) of 3-tert-butyl-4-(2-morpholin-4-ylethoxy)benzaldehyde as a yellowish oil.

Quelle