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Tetrahydrofuran → (e)-4-(3-Ethoxy-3-oxoprop-1-en-1-yl)benzoic acid

HRID 397059
ノート
印刷プレビュー

反応式

HRID 397059 の反応式
[CH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)=O.[C:12](P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:14][CH2:15][CH3:16])=[O:13].[OH-].[Na+].[CH2:38]1COCC1>O>[CH2:15]([O:14][C:12](/[CH:38]=[CH:1]/[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)=[O:13])[CH3:16]
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 4

HCID 8028TetrahydrofuranHCID 120884-Formylbenzoic acidHCID 14798Sodium HydroxideHCID 178473672HCID 178473672、化合物

生成物 1

HCID 11830959(e)-4-(3-Ethoxy-3-oxoprop-1-en-1-yl)benzoic acid収率 80%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a stirred solution of 4-formyl-benzoic acid (10.0 g, 66.7 mmol) in THF (140 ml) was added carboethoxytriphenylphosphorane (25.0 g, 71.8 mmol). To this solution was added NaOH (2.50 g, 66.7 mmol) as a solution in water (20 ml). The reaction was stirred at rt overnight. The reaction mixture was diluted with water (50 ml) and extracted with EtOAc (3×50 ml). The combined extracts were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, 5% MeOH/CH2Cl2) to give the desired compound as a white solid (11.68 g, 53.1 mmol, 80% yield).

後処理

  1. extractionextracted with EtOAc (3×50 ml)
  2. dry with materialThe combined extracts were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash chromatography (SiO2, 5% MeOH/CH2Cl2)

出典と根拠

ORDレコード
ord-46a0ac57e7c143718c004ac8116f8be7
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06608203B2

反応ノート

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