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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255857Generated: October 27, 2026

Tetrahydrofuran → HCID 178509794, compound

https://huagongshe.com/reaction/2255857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant(3-Fluoropropyl)triphenylphosphonium bromideHCID 11429580—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178509803HCID 178509803—
SolventWaterHCID 962—
ProductHCID 178509794HCID 17850979478.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A mixture of (3-fluoropropyl)triphenylphosphonium bromide (10.0 g, 24.8 millimols) with THF (50 ml) was cooled down to -20° C., followed adding t-BuOK (3.1 g, 27.3 millimols) to the mixture, stirring the resulting mixture for 30 minutes, dropwise adding to the mixture, a THF (60 ml) solution of trans-4-(4-cyanophenyl)cyclohexanecarbaldehyde (5.8 g, 27.3 millimols) so as to keep the temperature at -20° C. or lower, stirring the mixture at the same temperature for 2 hours, adding water (50 ml) to the reaction product after completion of the reaction, extracting the product with ethyl acetate (300 ml), three times washing the resulting organic layer with water, drying it over anhydrous magnesium sulfate, distilling off the solvent under reduced pressure, and subjecting the residue to silica gel column chromatography (eluent: toluene), to obtain raw 4-(trans-4-(4-fluorobutenyl)cyclohexyl)benzonitrile (5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05653911
Source datasetuspto-grants-1997_08
ORD IDord-21e80bffd2dd4ed097eaf0f4c85fbd68
Source noteuspto-grants-1997_08