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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247792Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/247792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt[1,1'-Biphenyl]-4,4'-dicarbonyl dichlorideHCID 75374—
Edukt(R)-(+)-1,1,1-Trifluoro-2-octanolHCID 2779099—
Edukt2-Fluoro-4-decyloxyphenolHCID 19013894—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt1,1,1Trifluoro-2-octyl 4-(2-fluoro-4-decyloxyphenyloxycarbonyl)biphenyl-4'-carboxylateHCID 19013909—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05207947
Quelldatensatzuspto-grants-1993_05
ORD IDord-0a71e7ba947049b6858dbe02c9b3e5ac
Quellennotizuspto-grants-1993_05