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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863368Generated: October 26, 2026

Tetrahydrofuran → HCID 178509794, compound

https://huagongshe.com/reaction/863368

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 by 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 numberUS05720899
Source datasetuspto-grants-1998_02
ORD IDord-beeb0fb6633140f888f50db746dceeaf
Source noteuspto-grants-1998_02