Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
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!

N-ETHYL 2-NITRO-4-(TRIFLUOROMETHYL)ANILINE synthesis

2synthesis methods
-

Yield:30377-62-9 72%

Reaction Conditions:

with triethylamine in N,N-dimethyl-formamide at 0 - 100; for 2 h;

Steps:

1 Step 1: Synthesis of N-ethyl-2-nitro-4-(trifluoromethyl) aniline

To a stirred solution of l-chloro-2-nitro-4-(trifluoromethyl)benzene (4 g, 17.69, mmol, 1 equiv.) in DMF(28 mL) were added TEA (5.36 mL, 53.07 mmol, 3equiv.) and ethylamine hydrochloride (1.74 g, 21.23 mmol, 1.2 equiv.) portion wise at 0°C. The resulting reaction mixture was stirred at 100°C for 2 h. After completion of reaction (monitored by TLC) was diluted with EtOAc (500 mL), and water (50 mL), The organic layer was separated and washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by combi-flash eluting with 0-60% EtOAc/hexane to give N-ethyl-2-nitro-4-(trifluoromethyl) aniline (3.0g, 12.81 mmol, 72% yield) as a yellow solid. LC-MS Method A: [M+H]+ = 235.1

References:

WO2022/133098,2022,A2 Location in patent:Page/Page column 95