1,1,1-Trifluorooctan-2-YL 6-hydroxynaphthalene-2-carboxylate → Benzoic acid, 4-((1-oxodecyl)oxy)-

HRID 1728527Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1728527
OC1C=C2C(=CC=1)C=C(C(OC(CCCCCC)C(F)(F)F)=O)C=C2.FC1C=C(O)C=CC=1C(OC(CCCCCC)C(F)(F)F)=O.C(O[C:57]1[CH:62]=C[C:60]([C:63]2C=C[C:66]([C:69]([O:71][C:72]3[CH:77]=[CH:76][C:75]([C:78]([O:80]C(CCCCCC)C(F)(F)F)=[O:79])=[C:74](F)[CH:73]=3)=[O:70])=[CH:65][CH:64]=2)=[CH:59][CH:58]=1)CCCCCCC>O1CCCC1>[CH2:66]([C:69]([O:71][C:72]1[CH:77]=[CH:76][C:75]([C:78]([OH:80])=[O:79])=[CH:74][CH:73]=1)=[O:70])[CH2:65][CH2:64][CH2:63][CH2:60][CH2:59][CH2:58][CH2:57][CH3:62]

Komponenten

5

Versuchsvorschrift

To a solution of the 1,1,1-trifluoro-2-octyl 6-hydroxynaphthalene-2-carboxylate (0.6 g) obtained in (1) above and the 4-n-nonylcarbonyloxybenzoic acid (0.45 g) obtained in (2) above in tetrahydrofuran (40 ml) were added dicyclohexylcarbodiimide (0.45 g) and dimethylaminopyridine (0.05 g). The solution was stirred overnight and distilled to remove the solvent. The residue was dissolved in dichloromethane (40 ml) and washed with dilute aqueous hydrochloric acid solution and water, in this order. The solution was dried over anhydrous magnesium sulfate and distilled to remove the solvent. The residue was purified by silica-gel column chromatography (developer: hexane/ethyl acetate=20/1) to obtain the titled compound (0.05 g) having specific rotation, [α]D20 =+42.86°.

Quellen und Nachweise

ORD-Eintrag
ord-bf0e1b7dd9604ca29b4be6f68913986c
Quelldatensatz
uspto-grants-1994_07
Patentnummer
US05328641

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