HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610850Generated: November 1, 2026
Triphenylphosphine → 1-Bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentene
https://huagongshe.com/reaction/610850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 4-(p-Chlorophenyl)-3-fluoro-4-methyl-2-penten-1-ol | HCID 54566349 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-Bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentene | HCID 54272913 | 92.6% |
Reaction Steps
A solution of triphenyl phosphine (12.58 g, 55.6 mmol) in carbon tetrachloride at -5° C. to 5° C. is treated dropwise with a solution of bromine (8.89 g, 55.6 mmol) in carbon tetrachloride over 50 minutes under nitrogen, stirred at room temperature for one hour, treated with a solution of 4-(p-chlorophenyl)-3-fluoro-4-methyl-2-penten-1-ol, (Z)- (10.6 g, 46.3 mmol) in carbon tetrachloride over 15 minutes, refluxed for 2.5 hours, cooled to room temperature, and poured into petroleum ether. The resultant mixture is filtered through diatomaceous earth and concentrated in vacuo to obtain a residue. Flash chromatography of the residue using silica gel and a 1:9 ethyl acetate/hexane solution gives the title product as an oil (12.5 g, 92.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998673 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-99126169dae6425c914c64338d36e623 |
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| Source note | uspto-grants-1999_12 |
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