HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-(Octyloxy)-2-(4-octylphenyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Iodooctane | HCID 12380 | — |
| Reactant | Diazabicyclo[5.4.0]undec-7-ene | HCID 9834010 | — |
| Reactant | 5-Hydroxy-2-(4-octylphenyl)pyrimidine | HCID 11529316 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(Octyloxy)-2-(4-octylphenyl)pyrimidine | HCID 14533391 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04906400 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-0a474cab7289496492172a707c2bc90c |
| Source note | uspto-grants-1990_03 |