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Sodium Hydroxide → N-(4-Aminophenyl)prop-2-enamide

HRID 1815909
ノート
印刷プレビュー

反応式

HRID 1815909 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[O:14])[CH:12]=[CH2:13])=[CH:6][CH:5]=1)([O-])=O.[OH-].[Na+]>CCOC(C)=O.O.[Fe]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([NH:10][C:11](=[O:14])[CH:12]=[CH2:13])=[CH:8][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 14798Sodium HydroxideHCID 82198N-(4-nitrophenyl)acrylamide

生成物 1

HCID 22496099N-(4-Aminophenyl)prop-2-enamide

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 962Water溶媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

A mixture of N-(4-nitrophenyl)-acrylamide (Step 1) (0.203 g, 1.06 mmol), Iron powder (0.354 g, 6.34 mmol), FeSO4 (0.587 g, 2.11 mmol), Celite® (0.2 g) and water (6 mL) was heated to reflux with stirring for 3 h. The reaction mixture was cooled to RT and the solution was made basic to pH 13-14 by the addition of 2 N NaOH. The reaction mixture was diluted with EtOAc and water. The solution was filtered to remove the solids and solids washed with EtOAc. The aqueous layer was extracted three times with EtOAc (25 mL) and the combined organics were dried over Na2SO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography using EtOAc as the solvent to give N-(4-aminophenyl)-acrylamide.

後処理

  1. temperaturewas heated
  2. temperatureto reflux
  3. filtrationThe solution was filtered
  4. customto remove the solids and solids
  5. washwashed with EtOAc
  6. extractionThe aqueous layer was extracted three times with EtOAc (25 mL)
  7. dry with materialthe combined organics were dried over Na2SO4
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. customThe residue was purified by column chromatography

出典と根拠

ORDレコード
ord-1df8ecf78fa64b2599bba770bcf7e4f8
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06881737B2

反応ノート

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