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Phenol → 2,2-Bis(4-hydroxyphenyl)propanoic acid

HRID 1456860
ノート
印刷プレビュー

反応式

HRID 1456860 の反応式
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:8]([OH:13])(=[O:12])[C:9]([CH3:11])=O.OS(O)(=O)=O>O>[OH:7][C:1]1[CH:6]=[CH:5][C:4]([C:9]([C:4]2[CH:5]=[CH:6][C:1]([OH:7])=[CH:2][CH:3]=2)([CH3:11])[C:8]([OH:13])=[O:12])=[CH:3][CH:2]=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 996PhenolHCID 1060Pyruvic AcidHCID 1118Sulfuric Acid

生成物 1

HCID 6566942,2-Bis(4-hydroxyphenyl)propanoic acid収率 48%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a cooled mixture of phenol (9.4 g, 0.1 mol), pyruvic acid (4.4 g, 0.05 mol), and water was added concentrated H2SO4 (4.5 mL, 18.0 g) dropwise with stirring. After 15 minutes the ice bath was removed and the reaction was warmed to room temperature and stirred for 18 hours. The reaction mixture was diluted with ethyl ether/water (200 ml 1:1) and the layers were separated. The organic layer was extracted with saturated aqueous NaHCO3. The aqueous extract was then acidified, extracted with ethyl ether, dried over MgSO4, filtered, and concentrated in vacuo to give 2,2-bis(4-hydroxyphenyl)propionic acid (6.2 g) as a colorless sticky oil.

後処理

  1. customAfter 15 minutes the ice bath was removed
  2. stirringstirred for 18 hours
  3. additionThe reaction mixture was diluted with ethyl ether/water (200 ml 1:1)
  4. customthe layers were separated
  5. extractionThe organic layer was extracted with saturated aqueous NaHCO3
  6. extractionThe aqueous extract
  7. extractionextracted with ethyl ether
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-02b3834ec4cb456dbb7a5bd75bbfa6b6
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05843968

反応ノート

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