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

HRID 847822Notes

Reaction equation

HRID 847822 reaction equation
[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]

Participants

5

Procedure

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 separted 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).

Workup

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

Sources & evidence

ORD record
ord-4e630529eae6433cb98d650ee014d48d
Source dataset
uspto-grants-1981_10
Patent number
US04293704

Reaction notes

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