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Water → 2-(4-Methoxyphenyl)prop-2-enoic acid

HRID 1859308
ノート
印刷プレビュー

反応式

HRID 1859308 の反応式
O[C:2]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)([CH3:6])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.O>O1CCOCC1>[CH3:14][O:13][C:10]1[CH:9]=[CH:8][C:7]([C:2](=[CH2:6])[C:3]([OH:5])=[O:4])=[CH:12][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 1118Sulfuric AcidHCID 131581022-Hydroxy-2-(4-methoxyphenyl)propanoic acid

生成物 1

HCID 145737872-(4-Methoxyphenyl)prop-2-enoic acid収率 78.2%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

2-Hydroxy-2-(4-methoxyphenyl)propionic acid (35 g, 178 mmol) was dissolved in dioxane (700 ml) and concentrated sulfuric acid (60 ml) was added thereto. The reaction mixture was refluxed for 2 hours under heating. The reaction solution was cooled and, after adding water, extracted with ethyl acetate. The organic layer was washed with saturated sodium thiosulfate solution and water, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 24.8 g (yield: 72%) of the title compound as a brown solid.

後処理

  1. temperatureThe reaction mixture was refluxed for 2 hours
  2. temperatureunder heating
  3. temperatureThe reaction solution was cooled
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with saturated sodium thiosulfate solution and water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-682fd67c9479434aa8ebc41887bd4154
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06153768

反応ノート

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