Réaction #2487439

ord-e161c0751dcc4d6ab09491ac4725617b

Équation de réaction

Cc1cccc(C#N)c1F
2-fluoro-3-methylbenzonitrile
O=C1CCC(=O)N1Br
NBS
CC(C)(C#N)N=NC(C)(C)C#N
AIBN
N#Cc1cccc(CBr)c1F
crude material
N#Cc1cccc(CBr)c1F
3-(Bromomethyl)-2-fluorobenzonitrile

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

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 2-fluoro-3-methylbenzonitrile (200 mg, 1.5 mmol) in 1,2-dichloroethane (30 ml) was added NBS (266 mg, 1.49 mmol) and AIBN (29 mg, 0.15 mmol) at RT. The reaction mixture was then heated to 80° C., and the reaction mixture was stirred for 2 h. After complete consumption of the starting material (by TLC), the reaction mixture was cooled to RT. The volatiles were removed under reduced pressure to obtain the crude material. Purification by silica gel column chromatography eluting with 2-3% EtOAc/hexane afforded compound I-6 (250 mg, 1.15 mmol, 78%) as colorless liquid. 1H NMR (500 MHz, CDCl3): δ 7.69-7.65 (m, 1H), 7.62-7.58 (m, 1H), 7.28-7.25 (m, 1H), 4.50 (s, 2H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08796001B2uspto-grants-2014_08