Hydrogen Bromide → 2-amino-5-bromo-N,3-dimethylbenzamide

HRID 490980ノート

反応式

HRID 490980 の反応式
[NH2:1][C:2]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([NH:6][CH3:7])=[O:5].[BrH:13].OO.S(=O)(O)[O-].[Na+].[OH-].[Na+]>O.C(O)(=O)C>[NH2:1][C:2]1[C:11]([CH3:12])=[CH:10][C:9]([Br:13])=[CH:8][C:3]=1[C:4]([NH:6][CH3:7])=[O:5]

参加物

8

反応物 5

HCID 260Hydrogen Bromide2 回HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 167706892-amino-N,3-dimethylbenzamide2 回HCID 23665763Sodium Bisulfite

生成物 1

HCID 442275752-amino-5-bromo-N,3-dimethylbenzamide

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒2 回

反応条件

温度
12 °C

実験手順

A mixture of 2-amino-N,3-dimethylbenzamide (i.e. the product of Step A of Example 5) (14 g, 85 mmol), acetic acid (50 mL), and water (50 mL) was cooled to 12° C., and concentrated hydrobromic acid (28.5 g, 0.34 mol) was added over 10 minutes at this temperature. Then 30% aqueous hydrogen peroxide (9 g, 0.08 mol) was added over 5 minutes at 10-11° C., and the mixture was allowed to warm slowly to room temperature while being stirred for 2.5 h. Then more concentrated hydrobromic acid (2.9 g) was added, and the mixture was stirred overnight at room temperature. To the mixture was then added water (50 mL) and sodium bisulfite (1.5 g), and then the pH was adjusted to 5-6 by the addition of 50% aqueous sodium hydroxide (˜15 mL). The mixture was filtered, and the solids were washed with water and dried in vacuo to afford the title compound, 19.5 g (94%).

後処理

  1. temperatureto warm slowly to room temperature
  2. stirringthe mixture was stirred overnight at room temperature
  3. filtrationThe mixture was filtered
  4. washthe solids were washed with water
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-172a301225ad4b1ab681ceeb8a41ae0d
出典データセット
uspto-grants-2009_05
特許番号
US07528260B2

反応ノート

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