![](/CAS/GIF/633327-49-8.gif)
N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide synthesis
- Product Name:N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide
- CAS Number:633327-49-8
- Molecular formula:C9H9FN2O3
- Molecular Weight:212.18
![2-AMINO-4-FLUORO-5-NITROTOLUENE](/CAS/GIF/633327-50-1.gif)
633327-50-1
79 suppliers
$35.00/5g
![Acetic anhydride](/CAS/20180808/GIF/108-24-7.gif)
108-24-7
5 suppliers
$14.00/250ML
![N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide](/CAS/GIF/633327-49-8.gif)
633327-49-8
21 suppliers
$60.00/100mg
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
![2-Acetamido-4-fluorotoluene](/CAS/GIF/366-49-4.gif)
366-49-4
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$55.00/250mg
![N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide](/CAS/GIF/633327-49-8.gif)
633327-49-8
21 suppliers
$60.00/100mg
![5-Fluoro-2-methylaniline](/CAS/GIF/367-29-3.gif)
367-29-3
272 suppliers
$7.00/5g
![N-(5-Fluoro-2-methyl-4-nitrophenyl)acetamide](/CAS/GIF/633327-49-8.gif)
633327-49-8
21 suppliers
$60.00/100mg