Hydrochloric Acid → 6-Amino-2,3,4-trimethoxybenzoic acid

HRID 536066ノート

反応式

HRID 536066 の反応式
[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[CH:9]=[C:8]2[C:4]=1[C:5](=[O:17])C(=O)[NH:7]2.[OH-:18].[Na+].OO.Cl>C(O)(=O)C>[NH2:7][C:8]1[C:4]([C:5]([OH:17])=[O:18])=[C:3]([O:2][CH3:1])[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[CH:9]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 132844034,5,6-Trimethoxy-1H-indole-2,3-dione

生成物 1

HCID 130363926-Amino-2,3,4-trimethoxybenzoic acid収率 28.2%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A solution of 4,5,6-tris(methyloxy)-1H-indole-2,3-dione (10 g, 42.2 mmol) in 33% aqueous NaOH (70.5 ml, 582 mmol) at 100° C. was treated with 30% aqueous hydrogen peroxide (12.9 ml, 126 mmol) dropwise over 30 min, at a rate to prevent the foaming mixture from overflowing the flask. After addition was complete, the mixture was stirred for 10 minutes before being cooled and diluted by the addition of ice. The mixture was adjusted to pH 8 by addition of concentrated HCl (70 mL) and then acidified to pH 3 with the addition of glacial acetic acid. The solid that formed was collected by filtration, washed with water, and dried under vacuum to give 6-amino-2,3,4-tris(methyloxy)benzoic acid (2.7 g, 28%) as a tan solid. MS (m/z) 228.0 (M+H+).

後処理

  1. additionAfter addition
  2. temperaturebefore being cooled
  3. additiondiluted by the addition of ice
  4. customThe solid that formed
  5. filtrationwas collected by filtration
  6. washwashed with water
  7. customdried under vacuum

出典と根拠

ORDレコード
ord-daf6a87a71b34302a5dd38d7bee06933
出典データセット
uspto-grants-2014_10
特許番号
US08859571B2

反応ノート

読み込み中…