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

HRID 482361
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 482361
[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
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Komponenten

5

Edukt 3

HCID 996PhenolHCID 1060Pyruvic AcidHCID 1118Sulfuric Acid

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-71b967fc88864fea9a04a0063a597fdb
Quelldatensatz
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05795900

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