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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Decyloxy)benzoic acid | HCID 138527 | — |
| Reactant | 4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenol | HCID 20082763 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 4-decyloxybenzoate | HCID 20082751 | 12.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05399291 |
|---|
| Source dataset | uspto-grants-1995_03 |
|---|
| ORD ID | ord-b90baab25ce34140820eaa526c210927 |
|---|
| Source note | uspto-grants-1995_03 |
|---|