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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247785Erstellt: 23. Oktober 2026

Benzoic acid, 4-((1-oxodecyl)oxy)- → 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate

https://huagongshe.com/de/reaction/247785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic acid, 4-((1-oxodecyl)oxy)-HCID 3608562—
Edukt1,1,1-Trifluoro-2-decyl 4-hydroxybenzoateHCID 14745754—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoateHCID 19013920—

Reaktionsschritte

To a solution of the 4-n-decanoyloxybenzoic acid (0.4 g) obtained in (3) and the 1,1,1-trifluoro-2-decyl 4-hydroxybenzoate (0.4 g) obtained in (2) in tetrahydrofuran (about 30 ml) were added dicyclohexylcarbodiimide (0.32 g) and dimethylaminopyridine (0.01 g). The mixture was stirred at room temperature for about 20 hours and was distilled to remove the solvent. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried over anhydrous magnesium sulfate and was distilled to remove the solvent. The residue was purified by silica-gel column chromatography (a developer : hexane/ethyl acetate=20/1) to obtain the titled compound (0.15 g). Phase transition temperatures (° C.) were observed under a polarization microscope using a hot stage as follows: ##STR53## where

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05207947
Quelldatensatzuspto-grants-1993_05
ORD IDord-6cfe97d6e01c4c83a1905e2fa8b45e0c
Quellennotizuspto-grants-1993_05