HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470090Generated: November 1, 2026
p-Bromoacetophenone → 4-Bromophenacyl bromide
https://huagongshe.com/reaction/1470090
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Bromophenacyl bromide | HCID 7454 | 67% |
Reaction Steps
Into a 250-mL 3-necked round-bottom flask, was placed a solution of 1-(4-bromophenyl)ethanone (10.0 g, 50.25 mmol, 1.00 equiv) in acetic acid (50 mL). This was followed by the addition of a solution of bromine (8.2 g, 1.05 equiv) in acetic acid (50 mL) dropwise with stirring at 60° C. over 90 min. The resulting solution was stirred for 3 h at 60° C. The resulting mixture was concentrated under vacuum. The crude product was re-crystallized from petroleum ether/ethyl acetate in the ratio of 7:1. This resulted in 9.3 g (67%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006281B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-5c033dc273cc45278ec78c52344a906c |
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| Source note | uspto-grants-2015_04 |
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