Reaktion #44656

Reaktionsgleichung

diisopropyl azodicarboxylate

(R)-1-[(3R,5R)-5-(4-chlorophenyl)morpholine-3-yl]ethanol

triphenylphosphine

4-nitrobenzoic acid

→

titled compound

Ausbeute 100.0%

4-nitrobenzoic acid (S)-1-[(3R,5R)-5-(4-chlorophenyl)morpholine-3-yl]ethyl ester

Ausbeute 100.0%

Lösungsmittel

water

ethyl acetate

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwhile cooling with ice
2. 2
   Sonstigethe organic layer was partitioned
3. 3
   WaschenThe organic layer was washed with brine
4. 4
   Trocknendried over anhydrous magnesium sulfate
5. 5
   SonstigeSolvent was removed by distillation under reduced pressure
6. 6
   Sonstigethe resulting residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→8/2→7/3)

Vorschrift

Under a nitrogen atmosphere, to a tetrahydrofuran (20 mL) solution containing (R)-1-[(3R,5R)-5-(4-chlorophenyl)morpholine-3-yl]ethanol (903 mg), triphenylphosphine (1.81 g) and 4-nitrobenzoic acid (1.16 g) was dropwise added diisopropyl azodicarboxylate (1.36 mL) while cooling with ice. The resultant solution was stirred at the same temperature for 30 minutes, and then at room temperature for 2 hours. The reaction solution was diluted with water and ethyl acetate, and the organic layer was partitioned. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate. Solvent was removed by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→8/2→7/3), to thereby obtain the titled compound (1.46 g). The physical properties of the compound were as follows.

Quelle