Nitric Acid → 3-Bromo-4-nitropyridine N-oxide

HRID 1982892ノート

反応式

HRID 1982892 の反応式
[N+:1]([O-:4])(O)=[O:2].[Br:5][C:6]1[CH:7]=[N+:8]([O-:12])[CH:9]=[CH:10][CH:11]=1.[OH-].[Na+]>S(=O)(=O)(O)O>[Br:5][C:6]1[CH:7]=[N+:8]([O-:12])[CH:9]=[CH:10][C:11]=1[N+:1]([O-:4])=[O:2]

参加物

5

反応物 3

HCID 944Nitric AcidHCID 14798Sodium HydroxideHCID 142763Pyridine, 3-bromo-, 1-oxide

生成物 1

HCID 5485213-Bromo-4-nitropyridine N-oxide収率 72%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒2 回

反応条件

温度
90 °C

実験手順

Concentrated nitric acid (128 ml) and concentrated sulfuric acid (77 ml) were slowly added to a solution of 3-bromopyridin-N-oxide (31.9 g, 181.0 mmol) prepared in Step 1 in concentrated sulfuric acid (77 ml), while maintaining the temperature at 0° C.˜5° C. The reaction mixture was stirred at 90° C. for 2 hours and then cooled to room temperature. The reaction mixture was added to 1000 ml of ice water, which was then brought to pH 8 with 50% sodium hydroxide solution. The resulting precipitate was filtered and dried to give the titled compound as a yellow solid (29.3 g, 72.0%).

後処理

  1. temperaturewhile maintaining the temperature at 0° C.˜5° C
  2. temperaturecooled to room temperature
  3. filtrationThe resulting precipitate was filtered
  4. customdried

出典と根拠

ORDレコード
ord-d38b85ffe98449859dbb57a838188dc3
出典データセット
uspto-grants-2009_06
特許番号
US07541366B2

反応ノート

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