HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499683Generated: October 31, 2026
Acetyl chloride → 1-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanone
https://huagongshe.com/reaction/1499683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Chloro-3-fluorophenol | HCID 2724523 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 1-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanone | HCID 16221436 | 126.2% |
Reaction Steps
To 4-chloro-3-fluorophenol (from Aldrich, 20 g, 100 mmol) was added acetyl chloride (14.1 mL, 199 mmol) under N2 with stirring. The resulting mixture turned into a clear solution at room temperature quickly and it was heated at 60° C. for 2 hours. To the resultant mixture was added aluminum trichloride (25.0 g, 187 mmol) in portions and the reaction mixture was heated at 180° C. for 30 minutes. The solids slowly dissolved at high temperature. The reaction mixture was then cooled to room temperature while the flask was swirled carefully in order for the solid to form a thin layer inside the flask and then slowly quenched with 1.0 N HCl (300 mL) while cooling in an ice-bath and stirred overnight. The yellow precipitate was washed with water and dried under vacuum to give the desired product as a yellow solid (23.8 g), which was directly used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-ae329b384d424f429e87e2f4986d853e |
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| Source note | uspto-grants-2015_12 |
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