HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 5-Butylpyridine-2-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Chloroacrylonitrile | HCID 70198 | — |
| Edukt | 1-Dimethylamino-1-aza-3-n-butyl-1,3-butadiene | HCID 86743901 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 5-Butylpyridine-2-carbonitrile | HCID 329377 | 63% |
Reaktionsschritte
0.1 mole of 1-dimethylamino-1-aza-3-n-butyl-1,3-butadiene, 0.1 mole of 2-chloroacrylonitrile and 0.2 mole of triethylamine are heated in 100 ml of acetonitrile for 20 hours to 60° C. The reaction mixture is concentrated by evaporation and the residue is dissolved in dioxane. The solution is filtered and gaseous HCl is introduced. The batch is stirred for 15 minutes at room temperature and then concentrated by evaporation. The residue is partitioned between CH2Cl2 and 1N NaHCO3. The organic phase is dried, concentrated by evaporation and distilled under a high vacuum, affording 10.0 g (63%) of a yellowish oil with a boiling point of 86°-87° C./3·10-1 mbar.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04923993 |
| Quelldatensatz | uspto-grants-1990_05 |
| ORD ID | ord-7db52327ff8b4b44938e3cd1c4358bb6 |
| Quellennotiz | uspto-grants-1990_05 |