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HCID 11074968, Verbindung → HCID 12011994, Verbindung

HRID 1937125
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1937125
[OH:1][C@H:2]1[C@@H:14]2[C@@H:10]([C:11](=[O:16])[O:12][C@H:13]2[CH3:15])[CH:9]=[C:8]2[C@@H:3]1[CH2:4][CH2:5][CH2:6][CH2:7]2>C(O)C.[Pt]=O>[OH:1][C@H:2]1[C@@H:14]2[C@@H:10]([C:11](=[O:16])[O:12][C@H:13]2[CH3:15])[CH2:9][C@@H:8]2[C@@H:3]1[CH2:4][CH2:5][CH2:6][CH2:7]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 11074968HCID 11074968, Verbindung

Produkt 1

HCID 12011994HCID 12011994, VerbindungAusbeute 96 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 82844Platinum oxide (PtO)KatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

To 375.1 mg(1.69 mmol) of (3S,3aS,4R,4aS,9aS)-4-hydroxy-3-methyl-3a,4,4a,5,6,7,8,9a-octahydronaphtho[2,3-c]furan-1(3H)-one in 5 ml of ethanol solution were added 40.0 mg(10% by weight) of platinum oxide, and catalytic reduction was conducted at ambient temperature under 98.1 Kpa. After stirring for 16 hours, the reaction mixture was filtered through celite and the residue was washed using 20 ml of ethyl acetate. Combined organic layers were distilled off under reduced pressure and the residue was purified by means of silica gel column chromtography(methylene chloride:ethyl acetate=4:1) to obtain 363.7 mg of (3S,3aS,4R,4aS,8aR,9aS)-4-hydroxy-3-methyl-decahydronaphtho[2,3-c]furan-1(3H)-one (yield 96%).

Aufarbeitung

  1. customwas conducted at ambient temperature under 98.1 Kpa
  2. filtrationthe reaction mixture was filtered through celite
  3. washthe residue was washed
  4. distillationCombined organic layers were distilled off under reduced pressure
  5. customthe residue was purified by means of silica gel column chromtography(methylene chloride:ethyl acetate=4:1)

Quellen und Nachweise

ORD-Eintrag
ord-ed99694a32bf4f3199fdecb508d9c81e
Quelldatensatz
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06392059B1

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