HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 2861892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 3999190 | HCID 3999190 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 2861892 | HCID 2861892 | 65.4% |
Reaction Steps
2-(m-Fluoro-p-hydroxyphenyl)-5-heptylpyridine (2 g, 0.007 mol), ethanol (20 ml), potassium hydroxide (0.48 g, 0.008 mol) and n-hexylbromide (1.4 g, 0.008 mol) were heated under reflux with stirring for 4 hours, followed by cooling the resulting reaction fluid, adding water and toluene, transferring the mixture into a separating funnel, washing the resulting organic layer with 2N-NaOH aqueous solution, then washing it with water, distilling off the solvent under reduced pressure, recrystallizing the residue from ethanol, filtering off it in a refrigerator and drying it to obtain the objective final product 2-(m-fluoro-p-hexyloxyphenyl)-5-heptylpyridine (1.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04781857 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-ca57ea1d4b35426f910ddd481d79385f |
| Source note | uspto-grants-1988_11 |