HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433936Generated: October 25, 2026
Hydrochloric Acid → 2-Chloro-1-(2,4-difluorophenyl)ethanone
https://huagongshe.com/reaction/433936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 1,3-Difluorobenzene | HCID 9741 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Chloro-1-(2,4-difluorophenyl)ethanone | HCID 588083 | 75% |
Reaction Steps
Into the solution of 1,3-difluorobenzene in 1,2-dicholoroethane (DCE) was added anhydrous aluminium chloride (1.2 molar equivalent of 1,3-difluorobenzene) at 25-30° C. and stirred for 30 minutes. The reaction mixture was then cooled to 0° C. and chloroacetyl chloride (1.1 molar equivalent of 1,3-difluorobenzene), in DCE, was then added into it over a period of 30-60 min keeping the reaction temperature below 20° C. After the addition was over, the reaction mixture was stirred at 25-30° C. for 5-7 hours. The reaction mixture was then diluted with DCE and poured into dil. hydrochloric acid (5%) at 0-5° C. The mixture was then extracted with DCE. The combined organic layer was washed successively with 5% aq. sodium bicarbonate solution and water. Evaporating DCE from the organic layer under reduced pressure gave an oil which on triturating with n-Hexane gave the title compound as white crystalline material (Yield 75% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670363B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-186f0a5f3da4434294b577da0c0bf1d7 |
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| Source note | uspto-grants-2003_12 |
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