StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Acetic Acid → 2-Cyclohexene-1,4-diyl Diacetate

HRID 1385762
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1385762
[C:1]([O-:4])(=[O:3])[CH3:2].[Li+].[C:6]1(=O)[CH:11]=[CH:10][C:9](=[O:12])[CH:8]=[CH:7]1.C1CCC=CC=1.[C:20](O)(=[O:22])[CH3:21]>CCCCC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.[O-2].[O-2].[Mn+4]>[C:1]([O:4][CH:6]1[CH2:7][CH2:8][CH:9]([O:12][C:20](=[O:22])[CH3:21])[CH:10]=[CH:11]1)(=[O:3])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 176Acetic AcidHCID 4650QuinoneHCID 116051,3-CyclohexadieneHCID 3474584Lithium acetate

Produkt 1

HCID 126964352-Cyclohexene-1,4-diyl DiacetateAusbeute 33 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 167845
palladium(II) acetate
Katalysator
HCID 178418406HCID 178418406, VerbindungKatalysator
HCID 8003PentaneLösungsmittel

Versuchsvorschrift

Lit., J. Org. Chem., 49:4619 (1984). To a stirred solution of 2.8 g (12.5 mmol) palladium acetate, 27.2 g (267 mmol) lithium acetate, and 7.64 g (70.7 mmol) benzoquinone in 200 ml acetic acid at room temperature were added 26.1 g (300 mmol) manganese dioxide and a solution of 23.8 ml (250 mmol) 1,3-cyclohexadiene in 400 ml pentane, and stirring continued for 16 h. The two-phase reaction mixture was separated and the acetic acid phase extracted twice with pentane. The combined organic extracts were washed successively with saturated brine, water, and 2 M sodium hydroxide solution, then the organic phases were dried over sodium sulphate and concentrated in vacuo. Recrystallisation from pentane afforded 16.1 g (33%) of the title compound as an off-white crystalline solid. MS m/e (%): 138 ([M−AcOH]+, 8), 96 ([M−AcOH—COCH2]+, 100), 43 (40).

Aufarbeitung

  1. customThe two-phase reaction mixture
  2. customwas separated
  3. extractionthe acetic acid phase extracted twice with pentane
  4. washThe combined organic extracts were washed successively with saturated brine, water, and 2 M sodium hydroxide solution
  5. dry with materialthe organic phases were dried over sodium sulphate
  6. concentrationconcentrated in vacuo
  7. customRecrystallisation from pentane

Quellen und Nachweise

ORD-Eintrag
ord-003a08c81d5743079000eddd05686288
Quelldatensatz
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06262089B1

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion