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N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide synthesis

3synthesis methods
-

Yield:633327-49-8 89%

Reaction Conditions:

at 15; for 36 h;Inert atmosphere;

Steps:

23 Preparation 23: /v-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide

5-fluoro-2-methyl-4-nitroaniline (9.5 g, 56 mmol) was added in portions to AC2O (100 mL) at 15 °C. The reaction mixture was stirred at about 15 °C for about 36 h. The solids were collected by filtration and rinsed with water (3 x 50 mL). The solids were dried to provide the title compound. Yield: 6.3 g. The filtrate was extracted with EtOAc (100 mL). The organic layer was washed with water (2 x 100 mL), sat. aq. Na2HCOs (3 x 100 mL), dried (Na2SC>4), filtered and concentrated. The crude product was purified by chromatography to provide additional title compound. Yield: 4 g. Both batches of MR (400

References:

WO2022/130171,2022,A1 Location in patent:Page/Page column 57