1,2-Dichloroethane → 2-Chlorovinyl 2,4-dichloro5-fluoro-phenyl ketone

HRID 981342Notes

Reaction equation

HRID 981342 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4](Cl)=[O:5].[Cl-].[Al+3].[Cl-].[Cl-].[Cl:17][CH2:18][CH2:19]Cl.C#C>C(Cl)Cl>[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4]([CH:19]=[CH:18][Cl:17])=[O:5]

Participants

6

Procedure

113.75 g (0.5 mole) of 2,4-dichloro-5-fluorobenzoyl chloride are added dropwise to a suspension of 73 g of anhydrous aluminum chloride and 200 ml of dry 1,2-dichloroethane at 0°-10° C., while cooling with ice and stirring. Acetylene is passed in at 40°-50° C. for 6.5 hours. The reaction mixture is poured onto ice, the organic phase is taken up in methylene chloride and the mixture is subsequently extracted with methylene chloride. After drying with sodium sulphate, the solvent is distilled off in vacuo. 121.7 g of 2-chlorovinyl 2,4-di-chloro-5-fluoro-phenyl ketone are obtained as a crude product of melting point 65°-70° C. Distillation under a fine vacuum gives 99.8 g (78.7%) of pure product of boiling point: 124°-128° C./0.1 mbar and melting point 71°-73° C.

Workup

  1. temperaturewhile cooling with ice
  2. additionThe reaction mixture is poured onto ice
  3. extractionthe mixture is subsequently extracted with methylene chloride
  4. dry with materialAfter drying with sodium sulphate
  5. distillationthe solvent is distilled off in vacuo

Sources & evidence

ORD record
ord-753bd001b5684b4790f07a1405d73829
Source dataset
uspto-grants-1991_02
Patent number
US04990646

Reaction notes

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