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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254942Generated: November 2, 2026

4-Fluorobenzaldehyde → HCID 178445612, compound

https://huagongshe.com/reaction/2254942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantHCID 178445610HCID 178445610—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDichloromethaneHCID 6344—
ProductHCID 178445612HCID 17844561280%

Reaction Steps

A solution of 2.4 g (0.01 mol) of 2-[2'-(trans-4"- butylcyclohexyl)ethyl]propane-1,3-diol, 1.8 g (0.01 mol) of 4-fluorobenzaldehyde (manufactured by Aldrich) and 0.1 g of TsOH in 50 cm3 of dichloromethane was refluxed for 3 hours over a hot water bath with a Dean-Stark trap. The resulting solution was washed with water and the dichloromethane was distilled off. The residue was recrystallized from a solvent mixture of acetone and methanol to yield 3.0 g (0.008 mol) of trans-2-(4'-fluorophenyl)-5-[2'-(trans-4"-butylcyclohexyl)ethyl]-1,3-dioxane. The phase transition temperature of this compound, measured by DSC, was: ##STR41## wherein C is the crystal phase, N is the nematic phase, and I is the isotropic liquid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05238599
Source datasetuspto-grants-1993_08
ORD IDord-04888a890d3e421ab05b0ab5dce39c44
Source noteuspto-grants-1993_08