HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272267Generated: October 25, 2026
Hydrochloric Acid → 1-(4-Bromo-2,5-difluorophenyl)ethan-1-one
https://huagongshe.com/reaction/272267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Bromo-1,4-difluorobenzene | HCID 67862 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 1-(4-Bromo-2,5-difluorophenyl)ethan-1-one | HCID 9991653 | 31% |
Reaction Steps
Anhydrous aluminum chloride was mixed (5 grams, 37.5 millimoles, 2.4 equivalents) with 1-bromo-2,5 difluorobenzene in a dry, round-bottom flask blanketed with nitrogen and fitted with a condenser. The mixture was heated to 60° C. and acetyl chloride (1.7 milliliters, 23.3 millimole, 1.5. equivalents) was added by syringe. The wet yellow solid changed then into a scarlet solution and was heated at 90° C. for 1 hour. The reaction mixture was poured onto 38 grams of ice, HCl was added (3 milliliters, 37% concentration) and the mixture was extracted with ether. The crude material was dried over magnesium sulfate and evaporated down. The crude material was purified by column chromatography or distilled. The product (1.2 grams, 31%) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456156B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-691c1f6113b0420b857c2890349e606a |
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| Source note | uspto-grants-2008_11 |
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