HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385643Generated: October 29, 2026
Triphenylphosphine → 1-(p-Chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropane
https://huagongshe.com/reaction/1385643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(4-Chlorophenyl)-1-(2-fluoro-3-hydroxyprop-1-enyl) cyclopropane | HCID 54354973 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(p-Chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropane | HCID 53765764 | 63% |
Reaction Steps
Under a nitrogen atmosphere, a solution of bromine (0.767 g, 4.8 mmol) in carbon tetrachloride at ice-water bath temperature is treated sequentially with a solution of triphenylphosphine (1.26 g, 4.8 mmol) in carbon tetrachloride and a solution of 3-[1-(p-chlorophenyl)-cyclopropyl]-2-fluoro-2-propen-1-ol, (Z)—(0.907 g, 4 mmol) in carbon tetrachloride, heated to and stirred at reflux for 70 minutes, cooled to room temperature, and poured into petroleum ether. The resultant mixture is filtered, and the filtrate is concentrated in vacuo to obtain a residue. The residue is dissolved in petroleum ether and passed through a plug of silica gel (eluted with hexanes) to obtain an oil. Flash column chromatography of the oil using silica gel and a 3:20 methylene chloride/hexanes solution gives the title product as a colorless oil (0.73 g, 63% yield) which is identified by NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262319B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-b051a02e5b6d4031a2147734b6c2ffb3 |
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| Source note | uspto-grants-2001_07 |
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