Reaktion #2254205

Reaktionsgleichung

2-[4-(4-fluorophenyl)oxan-4-yl]ethan-1-amine

benzaldehyde

→

benzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amine

Lösungsmittel

CH2Cl2

Reaktionsbedingungen

Aufarbeitung

1. 1
   FiltrationThe reaction mixture was filtered
2. 2
   Einengenconcentrated
3. 3
   workup.DISSOLUTIONThe residue was dissolved in 5 ml MeOH at 0° C.
4. 4
   workup.ADDITIONNaBH4 added in one portion (51 mg, 1.34 mmol)
5. 5
   workup.STIRRINGThe reaction was stirred at 0° C. for 1 h
6. 6
   SonstigeThe solution was then quenched with H2O (10 ml)
7. 7
   Extraktionextracted with CH2Cl2 (3×20 ml)
8. 8
   Waschenwashed with brine (10 ml)
9. 9
   Sonstigedried over NA2SO4
10. 10
    SonstigePurified by normal phase SiO2 chromatography (0 to 10% MeOH/CH2Cl2)

Vorschrift

To a solution of 2-[4-(4-fluorophenyl)oxan-4-yl]ethan-1-amine (250 mg, 1.12 mmol) in anhydrous CH2Cl2 (5 ml) and NA2SO4 (159 mg, 1.12 mmol) at rt was added benzaldehyde (0.17 ml, 1.68 mmol). The reaction was stirred overnight. The reaction mixture was filtered and concentrated. The residue was dissolved in 5 ml MeOH at 0° C. and NaBH4 added in one portion (51 mg, 1.34 mmol). The reaction was stirred at 0° C. for 1 h. The solution was then quenched with H2O (10 ml), extracted with CH2Cl2 (3×20 ml), washed with brine (10 ml) and dried over NA2SO4. Purified by normal phase SiO2 chromatography (0 to 10% MeOH/CH2Cl2) to give benzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amine as a colorless oil (200 mg, 60%, m/z: 314.2 [M+H]+ observed).

Quelle