Acetylene → 1-Chloro-trans-1-octen-3-one

HRID 225367

Reaktionsgleichung

Reaktionsgleichung von HRID 225367
[Cl-:1].[Al+3].[Cl-].[Cl-].[CH:5]#[CH:6].[C:7](Cl)(=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>C(Cl)(Cl)(Cl)Cl>[Cl:1]/[CH:5]=[CH:6]/[C:7](=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Komponenten

5

Versuchsvorschrift

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. (150 moles) of hexanoyl chloride. After the addition is complete, acetylene is bubbled into the mixture is 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.).

Aufarbeitung

  1. additionis added over 20 minutes 201.9 g
  2. additionAfter the addition
  3. customacetylene is bubbled into the mixture
  4. customis absorbed and for 1 hour
  5. customafter absorption
  6. additionThe mixture is poured onto 1700 g
  7. customThe organic phase is separated
  8. washthe aqueous phase is washed with ether
  9. washThe combined organic phase and washings are washed with saturated brine
  10. dry with materialdried (Na2SO4)
  11. customevaporated
  12. distillationof hydroquinone and distilled
  13. customto yield a colorless oil, b.p. 51°-52° C. (0.10 torr.)

Quellen und Nachweise

ORD-Eintrag
ord-fb7c836d1a0f4c95beebfdf7357e46fb
Quelldatensatz
uspto-grants-1980_11
Patentnummer
US04236027

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