HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543870Generated: November 1, 2026
p-Bromoacetophenone → 1-Bromo-4-(prop-1-en-2-yl)benzene
https://huagongshe.com/reaction/543870
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Triphenylmethyl phosphonium bromide | HCID 21951224 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-Bromo-4-(prop-1-en-2-yl)benzene | HCID 3614410 | 58.9% |
Reaction Steps
To a slurry of triphenylmethylphosphonium bromide (71.4 g, 200 mmole), in 500 ml dry THF at 0° C., were slowly added dropwise 135 ml (200 mmole) 1.44 M n-butyllithium in hexane. The mixture was stirred 30 minutes at 0° C., and a solution of 39.8 g (200 mmole) p-bromoacetophenone, in 100 ml dry THF, was slowly added dropwise. The mixture was allowed to warm slowly to ambient temperature, whereafter stirring was continued overnight. The stirred mixture was next filtered and the solvent removed by careful distillation at atmospheric pressure, the resulting residue was diluted with hexane, filtered, and the hexane removed by distillation. The remaining material was distilled, using a water aspirator vacuum, to produce 23.2 g (58.3% yield) of p-bromo-α-methylstyrene, bp 95°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04447542 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-2fd29c4ecfc743fc98fae64721d15d67 |
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| Source note | uspto-grants-1984_05 |
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