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Tetrahydrofuran → 7,8-Dimethyl-4,4a,5,6-tetrahydro-2(3H)-naphthalenone

HRID 478071
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 478071
C([N-][CH:5]([CH3:7])[CH3:6])(C)C.[Li+].C[C:10]1[C:11](=[O:17])[CH2:12][CH2:13][CH2:14][C:15]=1[CH3:16].[CH2:18]1COC[CH2:19]1>>[CH3:18][C:19]1[CH2:16][CH2:15][CH:14]2[C:7]([C:5]=1[CH3:6])=[CH:10][C:11](=[O:17])[CH2:12][CH2:13]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 8028Tetrahydrofuran2×HCID 2724682Lithium diisopropylamideHCID 108878982,3-Dimethyl-2-cyclohexen-1-one

Produkt 1

HCID 124539797,8-Dimethyl-4,4a,5,6-tetrahydro-2(3H)-naphthalenoneAusbeute 60 %

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a stirred solution of lithium diisopropylamide (LDA) (22 mmol) in THF (200 ml) at -78° C. was added a solution of 2,3-dimethylcyclohexenone (2.48 g, 20 mmol) in THF (50 ml). The mixture was warmed to 25° C., and the solvent and the amine were removed under vacuum. The resulting solid was dissolved in THF (400 ml) and the solution cooled to -78° C. To this solution was added MVK (1.8 ml, 22 mmol) in THF (100 ml) over 10 min. The resulting mixture was stirred 12 hr at room temperature, then worked up. Removal of solvent yielded the dione as a yellow oil (2.8 g, 60%).

Aufarbeitung

  1. customthe solvent and the amine were removed under vacuum
  2. dissolutionThe resulting solid was dissolved in THF (400 ml)
  3. temperaturethe solution cooled to -78° C
  4. additionTo this solution was added MVK (1.8 ml, 22 mmol) in THF (100 ml) over 10 min
  5. customRemoval of solvent

Quellen und Nachweise

ORD-Eintrag
ord-bbeec7b147a04622b97ec50f66b5c626
Quelldatensatz
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04889947

Notizen zur Reaktion

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