HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981342Generated: October 27, 2026
1,2-Dichloroethane → 2-Chlorovinyl 2,4-dichloro5-fluoro-phenyl ketone
https://huagongshe.com/reaction/981342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | 2,4-Dichloro-5-fluorobenzoyl chloride | HCID 2736821 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chlorovinyl 2,4-dichloro5-fluoro-phenyl ketone | HCID 54298666 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990646 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-753bd001b5684b4790f07a1405d73829 |
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| Source note | uspto-grants-1991_02 |
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