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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174447Generated: October 25, 2026

Water → beta-(4-(4-Propylcyclohexyl)cyclohexyl)-2-trifluoromethyl-3-fluoro-4-ethoxy styrene

https://huagongshe.com/reaction/1174447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantbeta-(4-(4-Propylcyclohexyl)cyclohexyl)-2-trifluoromethyl-3-fluoro-4-ethoxy-5-trimethylsilyl styreneHCID 86614748—
SolventTetrahydrofuranHCID 8028—
SolventTBAF tetrahydrofuranHCID 11078149—
Productbeta-(4-(4-Propylcyclohexyl)cyclohexyl)-2-trifluoromethyl-3-fluoro-4-ethoxy styreneHCID 67058734—

Reaction Steps

16.03 g of crude of β-(4-(4-propylcyclohexyl)cyclohexyl)-2-trifluoromethyl-3-fluoro-4-ethoxy-5-trimethylsilyl styrene was dissolved in 35 mL of THF, to which 23.4 mL of tetrabutyl ammonium fluoride/THF solution (1 mol/L) was dropped and stirred for 2 hours. The reaction solution was poured into 100 ml of water and extracted with 200 ml of toluene. The organic layer was washed with 100 ml of an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (eluent: heptane/toluene=8/2) and further recrystallized twice from a heptane/ethanol mixed solvent to obtain 7.89 g of β-(4-(4-propylcyclohexyl)cyclohexyl)-2-trifluoromethyl-3-fluoro-4-ethoxy styrene. The compound showed a liquid crystal phase and the transition points were as shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838087B2
Source datasetuspto-grants-2010_11
ORD IDord-c0e4cd7766c646cd83f2f40fabf11b85
Source noteuspto-grants-2010_11