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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650651Generated: October 27, 2026

Triethylamine → 4-(Hexyloxy)phenyl 4-(octyloxy)benzoate

https://huagongshe.com/reaction/1650651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-HexyloxyphenolHCID 29354—
Reactant4-Octyloxybenzoyl chlorideHCID 2760250—
SolventTetrahydrofuranHCID 8028—
Product4-(Hexyloxy)phenyl 4-(octyloxy)benzoateHCID 1591928950.4%

Reaction Steps

In tetrahydrofuran were dissolved 1.0 g of p-octyloxybenzoic acid chloride and 800 mg of p-hexyloxyphenol, and 500 mg of triethylamine was added to the solution and reaction was carried out with stirring overnight. The precipitate was removed by filtration, and the filtrate was concentrated, purified by using a silica gel column and recrystallized from ethanol to obtain 800 mg of 4-hexyloxyphenyl 4-octyloxybenzoate. The phase transition temperatures of the so-obtained compounds are as follows. ##STR142##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925591
Source datasetuspto-grants-1990_05
ORD IDord-dc559374cccd4f94ab3db8814e6b6147
Source noteuspto-grants-1990_05