Reacción #2487437

Ecuación de reacción

2,2′-azobis(isobutyronitrile)

6-methylnicotinonitrile

N-bromosuccinimide

→

crude material

6-(Bromomethyl)nicotinonitrile

Disolventes

1,2-dichloroethane

Condiciones de reacción

Tratamiento posterior

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

Procedimiento

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).

Fuente