Reaktion #476380

Reaktionsgleichung

bicarbonate

1-bromo-2,3-bis(bromomethyl)benzene

benzylamine

→

title compound

2-Benzyl-4-bromoisoindoline

Lösungsmittel

CH3CN

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe contents of the reaction flask were cooled
2. 2
   Filtrationfiltered
3. 3
   Sonstigethe solvent was removed by evaporation
4. 4
   Sonstigeand the mixture was partitioned between 1M K2CO3 and EtOAc
5. 5
   WaschenThe organic phases were washed with brine
6. 6
   Trocknendried with anhydrous Na2SO4
7. 7
   Filtrationfiltered
8. 8
   Sonstigeevaporated
9. 9
   WaschenFlash column chromatography (gradient elution: heptane to 10% EtOAc in heptane)

Vorschrift

Postassium bicarbonate (204 g, 2.04 mol) was suspended in CH3CN (12 L), and the mixture was heated to 80° C. Solutions of 1-bromo-2,3-bis(bromomethyl)benzene (280 g, 0.82 mol in 500 mL CH3CN) and benzylamine (87.5 g, 0.82 mol in 500 mL CH3CN) were added concurrently via addition funnels over 1 hour. The reaction mixture was then stirred at 77° C. for 16 hours. The contents of the reaction flask were cooled and filtered; the solvent was removed by evaporation; and the mixture was partitioned between 1M K2CO3 and EtOAc. The organic phases were washed with brine, dried with anhydrous Na2SO4, filtered, and evaporated. Flash column chromatography (gradient elution: heptane to 10% EtOAc in heptane) gave the title compound as a pale oil. 1H NMR (CDCl3) δ (ppm) 7.41-7.39 (m, 2H), 7.37-7.34 (m, 2H), 7.32-7.27 (m, 2H), 7.10-7.03 (m, 2H), 4.02 (s, 2H), 3.97 (s, 2H), 3.91 (s, 2H). LRMS (ESI) m/z 289 [(M+H)+; calcd for C15H15BrN: 289].

Quelle