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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728528Generated: October 25, 2026

4-Decanoyloxy-2-fluorobenzoic acid → 1,1,1-Trifluoro-2-decyl 4-hydroxybenzoate

https://huagongshe.com/reaction/1728528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Decanoyloxy-2-fluorobenzoic acidHCID 19365262—
Reactant3-Fluoro-4-(1,1,1-trifluoro-2-octyloxycarbonyl)phenyl 4-octyloxybiphenyl-4'-carboxylateHCID 53749937—
SolventTetrahydrofuranHCID 8028—
Product1,1,1-Trifluoro-2-decyl 4-hydroxybenzoateHCID 14745754—

Reaction Steps

To a solution of the 2-fluoro-4-n-nonylcarbonyloxybenzoic acid (0.3 g) obtained in (3) above and the 1,1,1-trifluoro-2-decyl 4-hydroxybenzoate (0.3 g) obtained in (2) above in tetrahydrofuran (about 30 ml) were added dicyclohexylcarbodiimide (0.25 g) and dimethylaminopyridine (0.02 g). The solution was stirred at room temperature for about 20 hours. The solution was distilled to remove the solvent. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried over anhydrone 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 (0.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328641
Source datasetuspto-grants-1994_07
ORD IDord-eaa54ae7bdf74895bf29218d0e8143c1
Source noteuspto-grants-1994_07