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Sodium Hydroxide → 3-Ethyl-3-(3-nitrophenyl)-4-pentenoic acid

HRID 397747
ノート
印刷プレビュー

反応式

HRID 397747 の反応式
[CH2:1]([C:3]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=1)([CH:9]=[CH2:10])[CH2:4][C:5]([O:7]C)=[O:6])[CH3:2].[OH-].[Na+]>C(O)(C)C>[CH2:9]([C:3]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=1)([CH:1]=[CH2:2])[CH2:4][C:5]([OH:7])=[O:6])[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 23000907Methyl 3-ethyl-3-(3-nitrophenyl)-4-pentenoate

生成物 1

HCID 230010243-Ethyl-3-(3-nitrophenyl)-4-pentenoic acid

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

実験手順

A solution of methyl 3-ethyl-3-(3-nitrophenyl)-4-pentenoate (Preparation 59, assume 7.25 mmol) in isopropyl alcohol (9 ml) and 2M aqueous sodium hydroxide solution (4.4 ml, 8.75 mmol) was heated under reflux for 11 h, then the reaction mixture was concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The phases were separated and the organic extract was dried (MgSO4), filtered and concentrated in vacuo to give the title compound as an oil which was used without further purification.

後処理

  1. temperatureunder reflux for 11 h
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. customThe residue was partitioned between ethyl acetate and water
  4. customThe phases were separated
  5. extractionthe organic extract
  6. dry with materialwas dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-89ff49498f134b0d84c637c9dce5d122
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06610711B2

反応ノート

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