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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247792Generated: October 25, 2026

Hydrochloric Acid → 1,1,1Trifluoro-2-octyl 4-(2-fluoro-4-decyloxyphenyloxycarbonyl)biphenyl-4'-carboxylate

https://huagongshe.com/reaction/247792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant[1,1'-Biphenyl]-4,4'-dicarbonyl dichlorideHCID 75374—
Reactant(R)-(+)-1,1,1-Trifluoro-2-octanolHCID 2779099—
Reactant2-Fluoro-4-decyloxyphenolHCID 19013894—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1,1,1Trifluoro-2-octyl 4-(2-fluoro-4-decyloxyphenyloxycarbonyl)biphenyl-4'-carboxylateHCID 19013909—

Reaction Steps

Into methylene chloride (20 ml) were added 4,4'-biphenyldicarboxylic acid chloride (0.5 g), (R)-(+)-1,1,1-trifluoro-2-octanol (0.15 g), triethylamine (0.09 g) and dimethylaminopyridine (0.03 g) and the mixture was left to stand for 8 hours in order to allow a reaction to proceed. Thereto were added 2-fluoro-4-decyloxyphenol (0.22 g) and triethylamine (0.09 g), and the mixture was left to stand for 8 hours in order to allow a reaction to proceed. The product was made acidic with 1N hydrochloric acid and extracted with methylene chloride. The extracted layer was washed with 1N aqueous sodium carbonate solution, water, aqueous sodium chloride solution (saturated) and water, in this order, until it was neutralized. After the product was dried over anhydrous magnesium sulfate, it was distilled under reduced pressure to remove the solvent. A solid product thus obtained was purified by silica-gel column chromatography until the titled compound (0.48 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05207947
Source datasetuspto-grants-1993_05
ORD IDord-0a71e7ba947049b6858dbe02c9b3e5ac
Source noteuspto-grants-1993_05