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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728527Generated: October 25, 2026

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

https://huagongshe.com/reaction/1728527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluorooctan-2-YL 6-hydroxynaphthalene-2-carboxylateHCID 15724811—
Reactant1,1,1-Trifluorooctan-2-YL 2-fluoro-4-hydroxybenzoateHCID 19920819—
Reactant3-Fluoro-4-(1,1,1-trifluoro-2-octyloxycarbonyl)phenyl 4-octyloxybiphenyl-4'-carboxylateHCID 53749937—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic acid, 4-((1-oxodecyl)oxy)-HCID 3608562—

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328641
Source datasetuspto-grants-1994_07
ORD IDord-bf0e1b7dd9604ca29b4be6f68913986c
Source noteuspto-grants-1994_07