Réaction #2487437

Équation de réaction

2,2′-azobis(isobutyronitrile)

6-methylnicotinonitrile

N-bromosuccinimide

→

crude material

6-(Bromomethyl)nicotinonitrile

Solvants

1,2-dichloroethane

Conditions de réaction

Traitement

1. 1
   AutreAfter complete consumption of the starting material (by TLC)
2. 2
   Températurethe reaction mixture was cooled to RT
3. 3
   Autrethe volatiles were removed under reduced pressure

Mode opératoire

To a stirred solution of 6-methylnicotinonitrile (1.0 g, 8.47 mmol) in 1,2-dichloroethane (30 mL) was added N-bromosuccinimide (NBS; 1.52 g, 8.54 mmol) and followed by 2,2′-azobis(isobutyronitrile) (AIBN; 0.14 g, 0.85 mmol) at RT. The reaction mixture was then heated to 80° C. and stirred for 14 h. After complete consumption of the starting material (by TLC), the reaction mixture was cooled to RT, and the volatiles were removed under reduced pressure to obtain the crude material. Purification by silica gel column chromatography eluting with 10% EtOAc/Hexane) afforded compound I-4 (0.6 g, 3.05 mmol, 36%) as a colorless liquid. 1H NMR (500 MHz, CDCl3): δ 7.67-7.62 (m, 2H), 7.21 (dd, J=9.0, 2.0 Hz, 1H), 4.44 (s, 2H).

Source