Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164766Generated: October 27, 2026

Ethanol → 5-(Octyloxy)-2-(4-octylphenyl)pyrimidine

https://huagongshe.com/reaction/1164766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-IodooctaneHCID 12380—
ReactantDiazabicyclo[5.4.0]undec-7-eneHCID 9834010—
Reactant5-Hydroxy-2-(4-octylphenyl)pyrimidineHCID 11529316—
SolventTolueneHCID 1140—
Product5-(Octyloxy)-2-(4-octylphenyl)pyrimidineHCID 1453339170%

Reaction Steps

To 5-hydroxy-2-(4-octylphenyl)pyrimidine (5 g, 0.018 mol) were added ethanol (50 ml), octyl iodide (12.6 g, 0.053 mol) and diazabicyclo[5.4.0]undec-7-ene (0.053 mol), followed by refluxing the mixture for 4 hours, dissolving the reaction mixture in toluene, sufficiently washing the solution with 2N-NaOH aqueous solution, further washing it with water, distilling off toluene and recrystallizing the residue from methanol (75 ml) to obtain 5-octyloxy-2-(4-octylphenyl)pyrimidine (5 g). This product exhibited liquid crystalline properties and its phase transition points were as follows: ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906400
Source datasetuspto-grants-1990_03
ORD IDord-0a474cab7289496492172a707c2bc90c
Source noteuspto-grants-1990_03