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ChemicalBook CAS DataBase List 2,2-DIMETHYL-7-NITRO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE
85160-83-4

2,2-DIMETHYL-7-NITRO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE synthesis

4synthesis methods
-

Yield:85160-83-4 348.6 g

Reaction Conditions:

with potassium carbonate in dimethyl sulfoxide at 26 - 30; for 24 h;

Steps:

1.1 (1)
Preparation of 2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-3(4H)-one

(1)
Preparation of 2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-3(4H)-one
To a solution of 2-amino-5-nitrophenol (200 g) in dimethylsulfoxide (1000 mL) was added anhydrous potassium carbonate (269 g) under stirring at 30°C or lower, then to the mixture was added ethyl 2-bromo-2-methylpropionate (278.4 g) at 30°C or lower, and the mixture was stirred at 26°C for 24 hours.
To the reaction mixture was added water (2000 mL) at 40°C or lower, and then stirred at room temperature for 3 hours.
The reaction product was collected by filtration, and successively washed with dimethylsulfoxide/water (2:1, 800 mL) and water (3200 mL) to obtain the title compound (348.6 g) as a yellow solid (wet material) (yield: 121%, purity: 96%).
MS: ESI-MS m/Z: 223 [M+H]+
1 H-NMR (CDCl3): δ 1.59 (6H, s), 6.95 (1H, d), 7.87 (1H, d), 7.92 (1H, dd), 9.38 (1H, brs)

References:

EP2883870,2015,A1 Location in patent:Paragraph 0073; 0074

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