Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974707Generated: October 30, 2026

2,4,5-Trichlorophenol → 2,4,5-Trichlorophenyl 4-n-Octyloxybenzoate

https://huagongshe.com/reaction/974707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrichlorophenolHCID 7271—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-(Octyloxy)benzoic acidHCID 17231—
SolventDiethyl EtherHCID 3283—
Product2,4,5-Trichlorophenyl 4-n-OctyloxybenzoateHCID 61620832%

Reaction Steps

To a solution of 4-octyloxybenzoic acid (13.8 g) in diethyl ether (552 ml) were added 2,4,5-trichlorophenol (10.87 g) and N,N'-dicyclohexylcarbodiimide (11.37 g). The solution was stirred under a nitrogen atmosphere for 18 hours at room temperature. The precipitate was removed by filtration, and the filtrate was concentrated in vacuo. The residue was dissolved in petroleum ether and was allowed to stand on ice-water. The resulting crystals (15.2 g) were filtered and dissolved in warm n-hexane (150 ml). After standing overnight at room temperature, the resulting crystals were removed by filtration. The filtrate was concentrated to an oil which was purified by a column chromatography (silica gel) using a mixture of ethyl acetate and n-hexane to give 2,4,5-trichlorophenyl 4-octyloxybenzoate (7.58 g) (m.p. 53° C., Anal: Calcd. for C21H23O3Cl3 :Cl24.75, Found: Cl 24.05).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0001638
Source datasetuspto-grants-1997_03
ORD IDord-446a916572ab4494a22d37635b12cd56
Source noteuspto-grants-1997_03