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Hydrogen Peroxide → 2-(1-Hydroxycyclopentyl)acetic acid

HRID 1586907
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1586907
[C@H:1]12[CH2:7][CH:4](CC1)[CH2:3][C:2]2=[O:8].[C:9]([O-:12])(=[O:11])[CH3:10].[Na+].OO>C(O)(=O)C>[OH:8][C:2]1([CH2:10][C:9]([OH:12])=[O:11])[CH2:3][CH2:4][CH2:7][CH2:1]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 784Hydrogen PeroxideHCID 517045Sodium AcetateHCID 54006847(1R)-Bicyclo(2.2.1)heptan-2-one

Produkt 1

HCID 3482662-(1-Hydroxycyclopentyl)acetic acidAusbeute 67 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

This product is oxidized by the Baeyer-Villiger procedure. (1R)-Norbornanone (81, 18 mmol) is stirred with sodium acetate (9 g, water-free), hydrogen peroxide (27 ml, 30%), and acetic acid (9 ml) at 5° C. in the dark for 40 hours. The reaction is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C. The product is extracted twice with EtOAc (600 ml). The extract is washed with the sodium sulfite solution, then with sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried and evaporated. The product is chromatographed on silica (380 g, ether) to yield the lacton of 3 hydroxycyclopentane-1-acetic acid (82, 12 mmol, 67%).

Aufarbeitung

  1. customThe reaction is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C
  2. extractionThe product is extracted twice with EtOAc (600 ml)
  3. washThe extract is washed with the sodium sulfite solution
  4. dry with materialwith sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried
  5. customevaporated
  6. customThe product is chromatographed on silica (380 g, ether)

Quellen und Nachweise

ORD-Eintrag
ord-7c2649edde5f475783fa29eb77f4d231
Quelldatensatz
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05216141

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