反应详情

Into a 100 mL round bottomed flask were added 5-bromonicotinoyl chloride (0.531 g, 2.41 mmol) and anhydrous pyridine (5 mL). A 2M solution of dimethylamine in THF (5 mL, 10.0 mmol) was added dropwise, and the reaction mixture was stirred at rt under N2 for 6 h after which it was concentrated under vacuum. The crude residue was partitioned between EtOAc and water. The layers were separated, and the organic phase was washed 3× with water, then treated with brine, dried (Na2SO4), filtered and concentrated to afford 5-Bromo-N,N-dimethyl-nicotinamide as a brown oil (0.4951 g, 89%). MS: m/z 229/231 [MH+].

1. concentrationwas concentrated under vacuum
2. customThe crude residue was partitioned between EtOAc and water
3. customThe layers were separated
4. washthe organic phase was washed 3× with water
5. additiontreated with brine
6. dry with materialdried (Na2SO4)
7. filtrationfiltered
8. concentrationconcentrated