反応 #2487437

ord-68d614573b8347ca8dea4f539c6437e7

反応方程式

CC(C)(C#N)N=NC(C)(C)C#N
2,2′-azobis(isobutyronitrile)
Cc1ccc(C#N)cn1
6-methylnicotinonitrile
O=C1CCC(=O)N1Br
N-bromosuccinimide
N#Cc1ccc(CBr)nc1
crude material
N#Cc1ccc(CBr)nc1
6-(Bromomethyl)nicotinonitrile

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After complete consumption of the starting material (by TLC)
  2. 2
    温度the reaction mixture was cooled to RT
  3. 3
    その他the volatiles were removed under reduced pressure

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08796001B2uspto-grants-2014_08