Ethanol → 4-Aminobenzene-1,3-dioic acid

HRID 1883078

反応式

HRID 1883078 の反応式
CCO.[N+:4]([C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=1[C:16]([OH:18])=[O:17])([O-])=O>[Pd].CC(O)=O>[NH2:4][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=1[C:16]([OH:18])=[O:17]

参加物

5

反応物 2

HCID 702EthanolHCID 30624384-Nitroisophthalic acid

生成物 1

HCID 113558524-Aminobenzene-1,3-dioic acid収率 75.1%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒

実験手順

Into 20 mL EtOH and 20 mL HOAc was dissolved 2 g (9.48 mmol) 4-nitroisophthalic acid, and the solution was subjected to hydrogenation at atmospheric conditions over 1 g of 5% Pd on carbon. After 16 h, mixture was filtered, and filtrate was evaporated. The residue crystallized from methylene chloride-hexane, giving 1.29 g (75%) crystalline desired intermediate.

後処理

  1. filtrationmixture was filtered
  2. customfiltrate was evaporated
  3. customThe residue crystallized from methylene chloride-hexane

出典と根拠

ORDレコード
ord-8a5f0be5b25d40afbfb21a32f965ad4a
出典データセット
uspto-grants-2004_07
特許番号
US06759414B2

関連ノート

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