3-Hydroxyanthranilic Acid → 2-Amino-5-bromo-3-hydroxybenzoic Acid

HRID 17512

反応式

HRID 17512 の反応式
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:4]([C:5]([OH:7])=[O:6])[C:3]=1[NH2:11].[Br:12]Br.CO.O>C(O)(=O)C>[NH2:11][C:3]1[C:2]([OH:1])=[CH:10][C:9]([Br:12])=[CH:8][C:4]=1[C:5]([OH:7])=[O:6]

参加物

6

反応物 4

HCID 863-Hydroxyanthranilic AcidHCID 887MethanolHCID 962WaterHCID 24408Bromine

生成物 1

HCID 217551432-Amino-5-bromo-3-hydroxybenzoic Acid収率 97%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

3-Hydroxyanthranilic acid (6.28 g, 41.0 mmol) was dissolved in acetic acid (550 ml), then a solution of bromine (13.1 g, 82.0 mmol) dissolved in acetic acid (50 ml) was gradually and dropwise added at room temperature, taking 20 minutes. After stirring at room temperature for 2.5 hours, methanol (70 ml) and water (300 ml) were added to the solution, followed by stirring at room temperature for 15 hours. The formed solid was collected by nitration, and dried under reduced pressure to obtain the entitled compound (9.129 g, 97%) as a brown powder.

後処理

  1. additiondropwise added at room temperature
  2. stirringby stirring at room temperature for 15 hours
  3. customThe formed solid was collected by nitration
  4. customdried under reduced pressure

出典と根拠

ORDレコード
ord-4ad1f4d15d514ec0aa6dbe5e8378817a
出典データセット
uspto-grants-2010_06
特許番号
US07737166B2

関連ノート

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