تفاعل #2487437

ord-68d614573b8347ca8dea4f539c6437e7

معادلة التفاعل

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

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter complete consumption of the starting material (by TLC)
  2. 2
    درجة الحرارةthe reaction mixture was cooled to RT
  3. 3
    أخرىthe volatiles were removed under reduced pressure

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08796001B2uspto-grants-2014_08