Réaction #312570
ord-d2de0c9643b54223baee8050e9ef6cc5
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1Concentrationconcentrated in vacuo
- 2workup.DISSOLUTIONThe residue was dissolved in CH2Cl2
- 3Lavagewashed with saturated aqueous NaHCO3 solution (100 mL)
- 4ExtractionThe aqueous layer was extracted with CH2Cl2 (2×50 ml)
- 5Concentrationthe organic layer was concentrated to an oil
- 6workup.DISSOLUTIONThis was dissolved in EtOAc which
- 7Autreto separate
- 8AutreThe EtOAc layer was separated
- 9Lavagewashed with saturated aqueous NaHCO3 solution (100 mL)
- 10ExtractionThe aqueous layer was extracted with EtOAc (2×50 ml)
- 11Lavagethe combined organic layer was washed with saturated aqueous NaCl solution (50 ml)
- 12Séchagedried over Na2SO4
- 13Filtrationfiltered
- 14Concentrationconcentrated to a crude orange liquid (3.77 g, ˜100%)
Mode opératoire
3-(2-Benzyl-2-aza-bicyclo[3.3.1]non-5-yl)-phenylamine (2.71 g, 8.84 mmol) stirred in pyridine (25 ml) at 0° C. was charged with 2-methoxy-ethanesulfonyl chloride (2.1 g, 13.26 mmol) dropwise causing a color change from yellow to bright orange. The reaction was allowed to warm to room temperature gradually and stirred 18 h. The reaction mixture was diluted with toluene and concentrated in vacuo. The residue was dissolved in CH2Cl2 and washed with saturated aqueous NaHCO3 solution (100 mL). The aqueous layer was extracted with CH2Cl2 (2×50 ml) and the organic layer was concentrated to an oil. This was dissolved in EtOAc which caused an oil to separate. The EtOAc layer was separated and washed with saturated aqueous NaHCO3 solution (100 mL). The aqueous layer was extracted with EtOAc (2×50 ml) and the combined organic layer was washed with saturated aqueous NaCl solution (50 ml), dried over Na2SO4, filtered and concentrated to a crude orange liquid (3.77 g, ˜100%). (TLC 75% EtOAc/hexanes Rf 0.48);