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103361-68-8

4-Methyl-6-nitro-2H-1,4-benzoxazin-3-one synthesis

5synthesis methods
-

Yield:103361-68-8 100%

Reaction Conditions:

Stage #1: 6-nitro-4H-benzo[1,4]oxazin-3-onewith sodium hydride in N,N-dimethyl-formamide at 0; for 0.166667 h;
Stage #2: methyl iodide in N,N-dimethyl-formamide at 0; for 1 h;

Steps:

8.2

Step 2; 4-Methyl-6-nitro-4H-benzo[1,4]oxazin-3-oneNaH (0.57 g, 23.75 mmol) was added to a solution of 6-nitro-4H-benzo[1,4]oxazin-3-one (2.3 g, 11.85 mmol) in DMF (50 ml) at 0° C. The mixture was stirred at 0° C. for 10 minutes and then CH3I (1.5 ml, 24.04 mmol) was added. The mixture was stirred at 0° C. for one hour, then at room temperature for one hour. The mixture was partitioned between EtOAc and water. The organic layer was dried (MgSO4), filtered, and concentrated under reduced pressure to give 2.5 g of 4-methyl-6-nitro-4H-benzo[1,4]oxazin-3-one as a solid, 100%.

References:

US2010/160373,2010,A1 Location in patent:Page/Page column 30