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Hydrogen Peroxide → 2-Amino-3-chloro-4-methoxybenzoic acid

HRID 420072
ノート
印刷プレビュー

反応式

HRID 420072 の反応式
[Cl:1][C:2]1[C:3]([O:13][CH3:14])=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9]C(=O)[C:7]2=[O:12].[OH-:15].[Na+].[Na+].[Cl-].OO>O.C(Cl)Cl>[NH2:9][C:10]1[C:2]([Cl:1])=[C:3]([O:13][CH3:14])[CH:4]=[CH:5][C:6]=1[C:7]([OH:12])=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 784Hydrogen PeroxideHCID 5234Sodium ChlorideHCID 14798Sodium HydroxideHCID 666505277-chloro-6-methoxy-1H-indole-2,3-dione

生成物 1

HCID 666505632-Amino-3-chloro-4-methoxybenzoic acid収率 36%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

A suspension of compound 103d (6.03 g, 28.52 mmol), NaOH (1.25 g, 31.37 mmol), and NaCl (3.49 g, 59.89 mmol) in water (60 mL) was stirred at room temperature for 30 min and was then ice-cooled. H2O2 was added dropwise. The mixture was stirred at 0° C. for 20 min and at room temperature for 3 hrs. The reaction mixture was quenched with glacial AcOH, filtered, and washed with water. The solid obtained was dissolved in DCM, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material was purified by chromatography on silica gel (DCM/MeOH) to yield compound 104d as an orange solid in 36% yield.

後処理

  1. temperatureice-cooled
  2. stirringThe mixture was stirred at 0° C. for 20 min and at room temperature for 3 hrs
  3. customThe reaction mixture was quenched with glacial AcOH
  4. filtrationfiltered
  5. washwashed with water
  6. customThe solid obtained
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe crude material was purified by chromatography on silica gel (DCM/MeOH)

出典と根拠

ORDレコード
ord-8345de03bd9c4a5eb8da0115f0dbe628
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093379B2

反応ノート

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