HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609435Generated: October 30, 2026
Triphenylphosphine → HCID 86748595, compound
https://huagongshe.com/reaction/1609435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzeneethanol, 4-bromo-3-fluoro- | HCID 20081205 | — |
| Reactant | 1331944-02-5 | HCID 20081208 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54176917 | HCID 54176917 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86748595 | HCID 86748595 | 42% |
Reaction Steps
Into a flask, were placed triphenylphosphine (2.9 g, 11 mmol) and 3-fluoro-4-bromophenethylbromide (2.2 g, 11 mmol) prepared from 3-fluoro-4-bromophenethylalcohol, followed by adding and dissolving xylene (15 ml), heating under reflux for 10 hours, adding THF (10 ml) to the reaction solution and stirring under ice-cooling, adding potassium-t-butoxid (1.1 g, 10 mmol) slowly to the reaction solution, stirring the reaction solution after the completion of dropping at room temperature for 2 hours, adding THF (10 ml) solution of 4-(ethylcyclohexyl) cyclohexylacetoaldehyde (2.4 g, 10 mmol), further stirring for 5 hours, adding ether after the completion of reaction, filtering off white solid deposited, concentrating the filtrate under reduced pressure, purifying the obtained brown oil by means of silica gel chromatography, to obtain a mixture (1.8 g, 4.2 mmol) of 1-(3-fluoro-4-bromophenyl)-4-(4-(4-ethylcyclohexyl)cyclohexyl)-2-Z-butene with its E-isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401434 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-12f8f418c13b4e889771525d3b33c7bf |
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| Source note | uspto-grants-1995_03 |
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