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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609435Generated: October 30, 2026

Triphenylphosphine → HCID 86748595, compound

https://huagongshe.com/reaction/1609435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzeneethanol, 4-bromo-3-fluoro-HCID 20081205—
Reactant1331944-02-5HCID 20081208—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54176917HCID 54176917—
SolventDiethyl EtherHCID 3283—
SolventO-XyleneHCID 7237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86748595HCID 8674859542%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401434
Source datasetuspto-grants-1995_03
ORD IDord-12f8f418c13b4e889771525d3b33c7bf
Source noteuspto-grants-1995_03