HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084549Generated: October 29, 2026
Acetic Acid → 4'-Bromo-3-chloropropiophenone
https://huagongshe.com/reaction/2084549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 4'-Bromo-3-chloropropiophenone | HCID 95790 | — |
Reaction Steps
45.3 g of aluminium chloride are stirred at room temperature in 80 ml of CH2Cl2. Maintaining vigorous stirring, a solution of β-propionic acid chloride (38.09 g, 28.7 ml, 0.3 mol) is poured slowly into 20 ml of CH2Cl2. The CH2Cl2-AlCl3-acid chloride complex forms quickly and the solution turns dark red. A solution of bromobenzene (47.1 g, 31.6 ml, 0.3 mol) is then introduced dropwise into 20 ml of CH2Cl2. The solution is then stirred for 15 hours at room temperature. The mixture is hydrolysed over 190 g of ice, to which 7.6 ml of concentrated acetic acid have been added. The organic phase is washed neutral and the solvent is removed by evaporation under reduced pressure. A dark red oil is obtained, from which the title compound is obtained in the form of a yellowish solid by extraction while hot with petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716852B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-b73e44bacae148178e6e18404f159493 |
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| Source note | uspto-grants-2004_04 |
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