Reaktion #95275

ord-332f2864e41a480dbb9cdb8d73153152

Reaktionsgleichung

C#C
acetylene
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
CCCCCC(=O)Cl
hexanoyl chloride
CCCCCC(=O)/C=C/Cl
1-chloro-trans-1-octen-3-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added over 20 minutes 201.9 g
  2. 2
    workup.ADDITIONAfter the addition
  3. 3
    Sonstigeacetylene is bubbled into the mixture as rapidly as it
  4. 4
    Sonstigeis absorbed and for 1 hour
  5. 5
    Sonstigeafter absorption
  6. 6
    workup.ADDITIONThe mixture is poured onto 1700 g
  7. 7
    SonstigeThe organic phase is separated
  8. 8
    Waschenthe aqueous phase is washed with ether
  9. 9
    WaschenThe combined organic phase and washings are washed with saturated brine
  10. 10
    Trocknendried (Na2SO4)
  11. 11
    Sonstigeevaporated
  12. 12
    workup.DISTILLATIONof hydroquinone and distilled
  13. 13
    Sonstigeto yield a colorless oil, b.p. 51°-52° C. (0.10 torr)

Vorschrift

To a slurry of 233.5 g. (1.75 moles) of aluminum chloride in 390 ml. of carbon tetrachloride, saturated with acetylene and cooled in an ice bath, is added over 20 minutes 201.9 g. (1.50 moles) of hexanoyl chloride. After the addition is complete, acetylene is bubbled into the mixture as rapidly as it is absorbed and for 1 hour after absorption becomes slow. The mixture is poured onto 1700 g. of ice and 720 ml. of saturated brine. The organic phase is separated and the aqueous phase is washed with ether. The combined organic phase and washings are washed with saturated brine, dried (Na2SO4) and evaporated. The residual oil is combined with 10 g. of hydroquinone and distilled to yield a colorless oil, b.p. 51°-52° C. (0.10 torr).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04343949uspto-grants-1982_08