Water → 2-Bromo-4-(tert-butyl)-6-nitroaniline

HRID 508321

反応式

HRID 508321 の反応式
[C:1]([C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[C:7]([N+:12]([O-:14])=[O:13])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[BrH:15].[NH+]1C=CC=CC=1.O.S([O-])([O-])=O.[Na+].[Na+]>C(O)(=O)C>[Br:15][C:10]1[CH:11]=[C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])[CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[C:8]=1[NH2:9]

参加物

6

反応物 4

HCID 962WaterHCID 24437Sodium SulfiteHCID 805734-tert-Butyl-2-nitroanilineHCID 21226041Pyridinium hydrobromide

生成物 1

HCID 509978562-Bromo-4-(tert-butyl)-6-nitroaniline収率 94%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A suspension of 4-tert-butyl-2-nitroaniline (1.033 g, 5.32 mmol) in glacial acetic acid (7.8 mL) was warmed with a heat gun until all solids had dissolved. The solution was then cooled and treated portion wise with pyridinium hydrobromide perbromide (1.96 g, 6.12 mmol). After addition, the solution was stirred at room temperature for 1 h. The mixture was added to water (50 mL) and treated with a small amount of sodium sulfite. After stirring for 30 min, the precipitate was collected by filtration. The solid obtained was washed with water and dissolved in EtOAc. Washed with water and brine. Dried over Na2SO4, filtered and concentrated under vacuum to provide the title compound as a yellow-orange solid (1.36 g, 94%).

後処理

  1. temperaturewas warmed with a heat gun until all solids
  2. dissolutionhad dissolved
  3. temperatureThe solution was then cooled
  4. additionAfter addition
  5. stirringAfter stirring for 30 min
  6. filtrationthe precipitate was collected by filtration
  7. customThe solid obtained
  8. washwas washed with water
  9. dissolutiondissolved in EtOAc
  10. washWashed with water and brine
  11. dry with materialDried over Na2SO4
  12. filtrationfiltered
  13. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-2cbc1eeeca104231a92bd89be3d30091
出典データセット
uspto-grants-2015_08
特許番号
US09095590B2

関連ノート

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