Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247793Generated: October 27, 2026

Hydrochloric Acid → 1,1,1-Trifluoro-2-decyl 4-(4'-decylbiphenyl-4-oxycarbonyl)-2,3,5,6-tetrafluorobenzoate

https://huagongshe.com/reaction/247793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant(R)-1,1,1-Trifluorodecan-2-olHCID 2779103—
Reactant2,3,5,6-Tetrafluorobenzene-1,4-dicarbonyl dichlorideHCID 13255340—
Reactant4-(4-Decylphenyl)phenolHCID 15084907—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1,1,1-Trifluoro-2-decyl 4-(4'-decylbiphenyl-4-oxycarbonyl)-2,3,5,6-tetrafluorobenzoateHCID 5421921441%

Reaction Steps

To methylene chloride (20 ml) were added 2,3,5,6-tetrafluoroterephthalic acid chloride (0.27 g), (R)-(+)-1,1,1-trifluoro-2-decanol (0.1 g), triethylamine (0.05 g) and dimethylaminopyridine (0.02 g). After the mixture was left to stand for 8 hours in order to allow a reaction to proceed, 4-decyl-4'-hydroxybiphenyl (0.15 g) and triethylamine (0.05 g) were added thereto. The mixture was left for about 8 hours in order to allow a reaction to proceed, made acidic with 1N aqueous hydrochloric acid solution and extracted with methylene chloride. The extracted layer was washed with lN aqueous sodium carbonate solution, water, aqueous sodium chloride solution (saturated) and water, in this order, to make it neutral. The layer was dried over anhydrous magnesium sulfate and distilled under reduced pressure in order to remove the solvent. The solid product obtained was purified by silica-gel column chromatography to obtain the titled compound (0.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05207947
Source datasetuspto-grants-1993_05
ORD IDord-a685d9e6e30e4f4f9ba847fbf878c135
Source noteuspto-grants-1993_05