Réaction #312573

Équation de réaction

3-(2-Benzyl-2-aza-bicyclo[3.3.1]non-5-yl)-benzonitrile

potassium carbonate

potassium carbonate

hydrogen peroxide

hydrogen peroxide

→

3-(2-Benzyl-2-aza-bicyclo[3.3.1]non-5-yl)-benzamide

Solvants

DMSO

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGstirred for 5.5 h
2. 2
   AutreAfter a water quench (50 ml)
3. 3
   Extractionthe product was extracted with EtOAc (3×50 ml)
4. 4
   Lavagewashed with 50% saturated aqueous NaCl solution (5×50 ml)
5. 5
   Séchagedried over Na2SO4
6. 6
   Filtrationfiltered
7. 7
   Concentrationconcentrated to a white solid which
8. 8
   Autrewas triturated with hexanes
9. 9
   Autrecollected (1.0 g, 49%)

Mode opératoire

3-(2-Benzyl-2-aza-bicyclo[3.3.1]non-5-yl)-benzonitrile (1.95 g, 6.16 mmol) in DMSO (55 ml) was charged with potassium carbonate (120 mg, 0.86 mmol) then 30% aqueous hydrogen peroxide (3.2 ml, 30.8 mmol). The reaction mixture was allowed to stir at room temperature for 23 h at which time it was determined not to have proceeded. Additional potassium carbonate (850 mg, 6.16 mmol) and 30% aqueous hydrogen peroxide (6.4 ml, 61.6 mmol) were introduced and stirred for 5.5 h. After a water quench (50 ml), the product was extracted with EtOAc (3×50 ml), washed with 50% saturated aqueous NaCl solution (5×50 ml), dried over Na2SO4, filtered and concentrated to a white solid which was triturated with hexanes and collected (1.0 g, 49%). (TLC 50% EtOAc/hexanes Rf 0.08); 1H NMR (400 MHz, CDCl3) δ 7.83-7.85 (m, 1H), 7.49-7.57 (m, 1H), 7.40-7.47 (m, 1H), 7.38 7.28 (m, 5H), 7.21 7.25 (m, 1H), 6.10 (brs, 1H), 5.63 (brs, 1H); 3.74-3.82 (m, 2H), 3.06-3.15 (m, 2H), 2.86-2.96 (m, 1H), 2.16 2.26 (m, 2H), 1.96 2.08 (m, 4H), 1.84-1.89 (m, 1H), 1.68 1.74 (m, 1H), 1.59 1.65 (m, 1H), 1.34-1.42 (m, 1H): APCl MS m/z 335.1 (M+1)+.

Source