Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 598176Erstellt: 24. Oktober 2026

Acetic Anhydride → (E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrile

https://huagongshe.com/de/reaction/598176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktEthyl orthoformateHCID 31214—
Edukt4-HeptanamineHCID 38665—
Edukt3-(2,6-Dichlorophenyl)-3-oxopropiononitrileHCID 3018140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrileHCID 6726733910,5%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 3-(2,6-dichlorophenyl)-3-oxopropanenitrile (0.200 g, 0.93 mmol), acetic anhydride (0.22 g, 2.20 mmol), and triethyl orthoformate (0.21 g, 1.40 mmol) was stirred at 150° C. for 1 hr. The solution was then concentrated and the residue redissolved in ethanol (5 mL). 4-heptylamine (0.16 g, 1.4 mmol) in 1 mL of tetrahydrofuran was added to the reaction mixture at 0° C. The reaction stirred for 30 minutes and was then concentrated. Flash chromatography (20% Ethyl acetate/hexanes) gave the desired compound (0.033 g, 10%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07897607B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-c02c2c1bc69342f3afc648452bc0ea63
Quellennotizuspto-grants-2011_03