Reaktion #351209

Reaktionsgleichung

p-Anisoyl chloride

N-phenyl-1,2-phenylenediamine

triethylamine

→

title compound

Ausbeute 62.2%

4-methoxy-N-(2-phenylaminophenyl)benzamide

Ausbeute 62.2%

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added dropwise over a 20 minute period
2. 2
   Temperaturwhile maintaining a temperature of <5° C
3. 3
   WaschenThe organic solution was washed successively with water (200 ml), 2N aqueous HCl (80 ml), and saturated brine solution (160 ml)
4. 4
   Trocknendried over sodium sulfate
5. 5
   WaschenThe silica was eluted with ethyl acetate (1 L)
6. 6
   Sonstigethe eluent was evaporated in vacuo to a pink solid
7. 7
   SonstigeThe solid was triturated overnight with ethyl ether (350 ml)
8. 8
   Temperaturcooled in an ice bath
9. 9
   Filtrationfiltered
10. 10
    Sonstigedried in vacuo

Vorschrift

A vigorously stirring solution of N-phenyl-1,2-phenylenediamine (20.15 g) in dichloromethane (325 ml) and triethylamine (11.07 g) was cooled in an ice/acetone bath under nitrogen. p-Anisoyl chloride (18.66 g) dissolved in dichloromethane (100 ml) was added dropwise over a 20 minute period while maintaining a temperature of <5° C. The reaction mixture was allowed to warm to ambient temperature and stirred for two hours. The organic solution was washed successively with water (200 ml), 2N aqueous HCl (80 ml), and saturated brine solution (160 ml), then dried over sodium sulfate and passed through a pad of silica (150 g). The silica was eluted with ethyl acetate (1 L) and the eluent was evaporated in vacuo to a pink solid. The solid was triturated overnight with ethyl ether (350 ml), cooled in an ice bath, filtered, and dried in vacuo to give the title compound as a light pink solid (21.67 g). 1H (300 MHz, CDCl3): d 3.82 (s, 3H), 5.75 (br s, 1H), 6.80-6.91(m, 5H), 7.12-7.29 (m, 5H), 7.62 (d, J=8.8 Hz, 2H), 8.15 (dd, J=1.7, 7.8 Hz, 1H), 8.36 (s, 1H); TLC (EtOAc/Hex, 1:4): Rf =0.24; m.p.: 148°-150° C.

Quelle