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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1650336Erstellt: 26. Oktober 2026

Triethylamine → 5-Butylpyridine-2-carbonitrile

https://huagongshe.com/reaction/1650336

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-ChloroacrylonitrileHCID 70198—
Edukt1-Dimethylamino-1-aza-3-n-butyl-1,3-butadieneHCID 86743901—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-Butylpyridine-2-carbonitrileHCID 32937763%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04923993
Quelldatensatzuspto-grants-1990_05
ORD IDord-7db52327ff8b4b44938e3cd1c4358bb6
Quellennotizuspto-grants-1990_05