反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([CH3:10])=[N:7][C:6]=2[CH:11]=1.S(=O)(=O)(O)O.[N+:17]([O-])([OH:19])=[O:18]>>[F:1][C:2]1[C:3]([N+:17]([O-:19])=[O:18])=[CH:4][C:5]2[O:9][C:8]([CH3:10])=[N:7][C:6]=2[CH:11]=1参加物
4
実験手順
5-Fluoro-2-methyl-benzoxazole (5.20 g, 0.0344 mol) was added to ice cooled Sulfuric acid (15.0 mL) such as to maintain the temperature below 25° C. After complete addition, a mixture of Sulfuric acid (2.75 mL) and Nitric acid (2.50 mL, 0.0536 mol) was added dropwise, maintaining the temperature below 18° C. After the addition was complete, the cooling bath was removed and the mixture was stirred at ambient temperature for 3 h, then was poured onto 100 mL ice with stirring. The solids were collected and washed with water (3×100 mL) and dried to give 5-Fluoro-2-methyl-6-nitro-benzoxazole as yellow solids. 1H-NMR (DMSO): 8.64 (d, 1H, J=5.4 Hz), 7.97 (d, 1H, J=10.8 Hz), 2.71 (s, 3H).
後処理
- temperatureto maintain the temperature below 25° C
- additionAfter complete addition
- additionwas added dropwise
- temperaturemaintaining the temperature below 18° C
- additionAfter the addition
- customthe cooling bath was removed
- additionwas poured onto 100 mL ice
- stirringwith stirring
- customThe solids were collected
- washwashed with water (3×100 mL)
- customdried
出典と根拠
- ORDレコード
- ord-f3e0e7316dfb4103befc1133ecc94197
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08552186B2
関連ノート
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