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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638948Generated: October 27, 2026

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

https://huagongshe.com/reaction/1638948

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, sufficeiently washing the solution with 2N--NaOH aqueous solution, further washing it with water, distilling off toluene and recrystallizing the residue from ethanol (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:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882083
Source datasetuspto-grants-1989_11
ORD IDord-918eda9561f44613917e0d0f992ed515
Source noteuspto-grants-1989_11