HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855268Generated: October 28, 2026
p-Bromoacetophenone → 1-Bromo-4-(prop-1-en-2-yl)benzene
https://huagongshe.com/reaction/855268
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Phosphine, triphenyl-, hydrobromide | HCID 517696 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Bromo-4-(prop-1-en-2-yl)benzene | HCID 3614410 | 53% |
Reaction Steps
To a solution of triphenylphosphonium bromide (17.94 g, 50.24 mmol) in DMSO (10 ml) was added n-BuLi (39.25 ml, 1.6M solution in hexane, 62.80 mmol). The solution was stirred at rt for 1 h and to this was added a solution of 4-bromoacetophenone (10.00 g, 50.24 mmol) in DMSO (4 ml). The reaction mixture was then stirred at rt overnight and then quenched with water and the product was extracted with pentane. The organic layers were combined washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by filtration through a short pad of silica using pentane as eluant to give 1-bromo-4-isopropenylbenzene (5.23 g, 53%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ 7.45 (d, J=9.0 Hz, 2H), 7.32 (d, J=9.0 Hz, 2H), 5.36 (m, 1H), 5.10 (m, 1H), 2.12 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259183B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-79570d942cfa40f5aed0615cfbfef6d1 |
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| Source note | uspto-grants-2007_08 |
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