Reaktion #1660

ord-a87607fbb9ca412d85516fecfc51ea39

Reaktionsgleichung

C#CC1CCCCC1
cyclohexylacetylene
C=O
formaldehyde
C=O
paraformaldehyde
OCC#CC1CCCCC1
3-cyclohexyl-2-propyn-1-ol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture was refluxed for 2 hours
  2. 2
    Sonstigewas bubbled into the mixture
  3. 3
    TemperaturAfter cooling
  4. 4
    Sonstigethe reaction was quenched with saturated ammonium chloride
  5. 5
    Extraktionextracted with ether (2×100 ml)
  6. 6
    WaschenThe combined ether extracts were washed with brine
  7. 7
    Trocknendried over magnesium sulfate
  8. 8
    Sonstigeevaporated
  9. 9
    Sonstigeto yield the product which
  10. 10
    workup.DISTILLATIONwas distilled under high vacuum at 68°-74° C.
  11. 11
    Sonstigeto yield 6.4 g as a colorless liquid

Vorschrift

To a solution of ethyl magesium bromide (prepared from 2.5 g of magnesium turning and 11.3 g of bromoethane) in ether was added dropwise a solution of 10.2 g of cyclohexylacetylene in ether and the reaction mixture was refluxed for 2 hours. The reaction mixture was cooled to ambient temperature and anhydrous formaldehyde (prepared from the thermal decomposition of 50 g of paraformaldehyde for 20 minutes) was bubbled into the mixture. After cooling, the reaction was quenched with saturated ammonium chloride and extracted with ether (2×100 ml). The combined ether extracts were washed with brine, dried over magnesium sulfate and evaporated to yield the product which was distilled under high vacuum at 68°-74° C. to yield 6.4 g as a colorless liquid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726176uspto-grants-1998_03