Reaktion #2022011

Reaktionsgleichung

N-(4-chloro-2-fluoro-5-nitrophenyl)acetamide

→

title compound

Ausbeute 93.3%

N-(5-Amino-4-chloro-2-fluorophenyl)acetamide

Ausbeute 93.3%

Lösungsmittel

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe autoclave was purged two times with nitrogen at 500 kPa (5 atmospheres)
2. 2
   TemperaturAfter 6 hours the autoclave was cooled to room temperature
3. 3
   FiltrationThe catalyst was filtered off
4. 4
   Sonstigethe solvent removed under reduced pressure
5. 5
   SonstigeThe solid was triturated with petroleum ether
6. 6
   Filtrationfiltered

Vorschrift

In a 1 L autoclave, 23.25 g (0.1 mole) of N-(4-chloro-2-fluoro-5-nitrophenyl)acetamide and 1.2 g of Ni-catalyst were suspended under nitrogen in 500 mL of ethyl acetate. The autoclave was purged two times with nitrogen at 500 kPa (5 atmospheres) and once with hydrogen at 500 kPa (5 atmospheres). 500 kPa (5 atmospheres) of hydrogen was then applied and the reactor heated to 75-80° C. After 6 hours the autoclave was cooled to room temperature. The catalyst was filtered off and the solvent removed under reduced pressure. The solid was triturated with petroleum ether and filtered to give 18.9 g of the title compound as a crystalline solid melting at 142-143° C. (purity: 99.4% by HPLC).

Quelle