4-(2-Propenyl)-2-cyclohexen-1-one → (3R,4S)-3-Methyl-4-(prop-2-en-1-yl)cyclohexan-1-one

HRID 1650065

Reaktionsgleichung

Reaktionsgleichung von HRID 1650065
[Li].[CH3:2][Cu]C.[CH2:5]([CH:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH:10]=[CH:9]1)[CH:6]=[CH2:7]>O1CCCC1>[CH3:2][C@H:9]1[C@H:8]([CH2:5][CH:6]=[CH2:7])[CH2:13][CH2:12][C:11](=[O:14])[CH2:10]1

Komponenten

4

Edukt 2

HCID 109535714-(2-Propenyl)-2-cyclohexen-1-oneHCID 178477771HCID 178477771, Verbindung

Produkt 1

HCID 15670663(3R,4S)-3-Methyl-4-(prop-2-en-1-yl)cyclohexan-1-oneAusbeute 55 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a 0° C. solution of 0.282 mole of dimethyl copper lithium in 200 ml. of tetrahydrofuran was slowly added a solution of 25.6 g. (0.188 mole) of 4-(2-propenyl)cyclohex-2-en-1-one in 50 ml. of tetrahydrofuran. The reaction was stirred 15 minutes and then quenched by addition to a 0° C. saturated solution (500 ml.) of ammonium chloride. The quenched reaction was extracted with 500 ml. ether. The ether extract was washed with 500 ml. saturated ammonium chloride, dried over magnesium sulfate and evaporated to an oil which was purified via distillation to yield 15.5 g. (55%) of the title compound.

Aufarbeitung

  1. customTo a 0° C.
  2. customquenched by addition to a 0° C. saturated solution (500 ml.) of ammonium chloride
  3. customThe quenched reaction
  4. extractionwas extracted with 500 ml
  5. extractionThe ether extract
  6. washwas washed with 500 ml
  7. dry with materialsaturated ammonium chloride, dried over magnesium sulfate
  8. customevaporated to an oil which
  9. distillationwas purified via distillation
  10. customto yield 15.5 g

Quellen und Nachweise

ORD-Eintrag
ord-c5022e69a40a4905bde04a4e2673a688
Quelldatensatz
uspto-grants-1990_05
Patentnummer
US04921994

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