Reacción #304673

Ecuación de reacción

2-iodo-5-(trifluoromethyl)benzonitrile

(5-isopropyl-2-methoxyphenyl)boronic acid

Na2CO3

ethanol

→

5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-carbonitrile

Disolventes

dimethyl ethylene glycol

water

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe solution was degassed with nitrogen for 2 minutes
2. 2
   Otrothe solution was degassed with nitrogen again for 2 minutes
3. 3
   OtroEach tube was degassed with nitrogen for 1 minute
4. 4
   Otrosealed
5. 5
   Otroplaced in a microwave reactor
6. 6
   Otroreached 150° C.
7. 7
   workup.WAITthe temperature was held at 150° C. for ten minutes
8. 8
   workup.ADDITIONpoured into H2O (50 mL)
9. 9
   Extracciónextracted with EtOAc (100 mL)
10. 10
    LavadoThe organic layer was washed with brine (50 mL)
11. 11
    Secadodried over Na2SO4
12. 12
    Filtraciónfiltered
13. 13
    Concentraciónconcentrated
14. 14
    OtroPurification by flash chromatography with 15% CH2Cl2/hexanes

Procedimiento

To a solution of 2-iodo-5-(trifluoromethyl)benzonitrile (2.0 g, 6.7 mmol) and (5-isopropyl-2-methoxyphenyl)boronic acid (1.6 g, 8.4 mmol) in dimethyl ethylene glycol (30.4 mL) was added 2M Na2CO3 (6.8 mL), ethanol (9.6 mL), and water (10 mL). The solution was degassed with nitrogen for 2 minutes. Pd(PPh3)4 (774 mg, 0.67 mmol) was added and the solution was degassed with nitrogen again for 2 minutes. The solution was divided equally into two 40 mL microwave tubes. Each tube was degassed with nitrogen for 1 minute, sealed, and placed in a microwave reactor. The wattage was set for 200 W until the temperature reached 150° C. and then the temperature was held at 150° C. for ten minutes. The tubes were then cooled to room temperature, combined, poured into H2O (50 mL), and extracted with EtOAc (100 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 15% CH2Cl2/hexanes afforded 5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-carbonitrile as a light yellow oil. Rf=0.65 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.97 (s, 1H), 7.85 (d, J=8.0 Hz, 1H), 7.63 (d, J=8.0 Hz, 1H), 7.31 (dd, J=8.5, 2.0 Hz, 1H), 7.12 (d, J=2.0 Hz, 1H), 6.97 (d, J=8.5 Hz, 1H), 3.82 (s, 3H), 2.93 (m, 1H), 1.27 (d, J=7.0 Hz, 6H).

Fuente