Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

345-30-2

N-(3-fluoro-4-nitrophenyl)acetamide synthesis

6synthesis methods
-

Yield:345-30-2 91%

Reaction Conditions:

at 22; for 16 h;Inert atmosphere;

Steps:

47 Preparation 47: N-(3-fluoro-4-nitrophenyl)acetamide

3-Fluoro-4-nitroaniline (20 g, 128.1 mmol) was treated with Ac2O (250 ml_). The mixture was stirred for 16 h at RT and then diluted with water (100 ml_). The precipitate was collected by filtration. The solids were taken up in EtOAc (100 ml_), dried (Na2SO4), filtered and concentrated to give the title compound 47 (23.0 g, 91% yield).1H NMR(400 MHz, CD3OD) d 8.09 (t, 1 H), 7.86 (dd, 1 H), 7.38 (dt, 1 H), 2.17 (s, 3H).

References:

WO2021/124155,2021,A1 Location in patent:Page/Page column 53; 76