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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608902Generated: October 30, 2026

4-(Decyloxy)benzoic acid → 4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 4-decyloxybenzoate

https://huagongshe.com/reaction/1608902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Decyloxy)benzoic acidHCID 138527—
Reactant4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenolHCID 20082763—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 4-decyloxybenzoateHCID 2008275112.1%

Reaction Steps

0.45 g (0.0016 moles) of 4-decyloxybenzoic acid and 0.58 g (0.0016 moles) of 4-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenol (prepared essentially as in Example 5) were dissolved in 25 ml of methylene chloride. N,N-dicyclohexylcarbodiimide (0.35 g, 0.0017 moles) was added to the reaction mixture, followed by 0.05 g of 4-(N,N-dimethylamino)pyridine. The resultant mixture was stirred at room temperature under nitrogen for 18 hours. The resulting urea precipitate was removed from the product solution by filtration, and the filtrate was concentrated on a rotary evaporator at reduced pressure. The crude product was purified by flash chromatography on silica gel (chloroform) to yield 0.12 g of 4-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 4-decyloxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399291
Source datasetuspto-grants-1995_03
ORD IDord-b90baab25ce34140820eaa526c210927
Source noteuspto-grants-1995_03