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Sodium Sulfite → HCID 178518956、化合物

HRID 268852
ノート
印刷プレビュー

反応式

HRID 268852 の反応式
[Br:1][C:2]1[C:3]([C:9]([OH:11])=O)=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].[N:12]([O-])=O.[Na+].[O-]S([O-])=O.[Na+].[Na+]>O.Cl>[Br:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:4]2[C:3]=1[C:9]([OH:11])=[N:12][NH:5]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 24437Sodium SulfiteHCID 105606492-Amino-6-bromobenzoic acidHCID 23668193Sodium Nitrite

生成物 1

HCID 178518956HCID 178518956、化合物収率 49%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒2 回HCID 962Water溶媒3 回

反応条件

温度
0 °C

実験手順

To a mixture of 3-bromo-2-carboxyaniline (6.6 g, 30.6 mmol, see Aust. J. Chem., 1999, 52, 1061) in H2O (28 ml) and HCl (conc., 6 ml) was added a solution of NaNO2 (2.11 g, 30 mmol) in H2O (5 ml) at 0° C. The mixture was stirred at 0° C. for 30 minutes then a solution of Na2SO3 (10.4 g, 82.5 mmol) in H2O (28 ml) was added slowly. The mixture was stirred at room temperature for 2 hours and HCl (conc., 9 ml) was slowly added. The resulting mixture was stirred at room temperature for additional 18 hours, then at 80° C. for 4 hours, and finally cooled to room temperature. The reaction mixture was basified to dissolve the precipitate and then reacidified. The precipitated 4-Bromo-1H-indazol-3-ol CLXXXIII was filtered and dried in vacuo (yellow powder, 3.19 g, 49% yield).

後処理

  1. stirringThe mixture was stirred at room temperature for 2 hours
  2. stirringThe resulting mixture was stirred at room temperature for additional 18 hours
  3. waitat 80° C. for 4 hours
  4. temperaturefinally cooled to room temperature
  5. dissolutionto dissolve the precipitate
  6. filtrationThe precipitated 4-Bromo-1H-indazol-3-ol CLXXXIII was filtered
  7. customdried in vacuo (yellow powder, 3.19 g, 49% yield)

出典と根拠

ORDレコード
ord-bf14a856c4104ba7a1e0dd3454d00cd6
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446118B2

反応ノート

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