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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 426166Erstellt: 23. Oktober 2026

Benzaldehyde, 3,5-dimethyl- → 3-(3,5-Dimethyl-phenyl)-acrylonitrile

https://huagongshe.com/de/reaction/426166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehyde, 3,5-dimethyl-HCID 34225—
EduktDiethyl (cyanomethyl)phosphonateHCID 75676—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3,5-Dimethyl-phenyl)-acrylonitrileHCID 6670545394,3%

Reaktionsschritte

To a stirred mixture of 3,5-dimethyl benzaldehyde (13.4 g, 0.1M), diethyl cyanomethylphosphonate (19.4 g, 0.11M) in anhydrous THF (200 ml) under nitrogen at 0° C. (ice bath), was added potassium t-butoxide (12.3 g, 0.11M). After stirring for 1 hr., the mixture was stirred for overnight at room temperature. The mixture was then partitioned between ether and water. The ether layer was taken, dried with anhydrous magnesium sulfate, filtered, evaporated in vacuo, and the residue was purified by silica gel column chromatography (eluent, ether:hexanes (1:20)) to afford 14.8 g (86%) of a white solid. m.p. 67-68° C.; 1H NMR (200 MHz, CDCl3) δ 2.33 (6H, s), 5.83 (1H, d, J=16.6 Hz), 7.05 (3H, s), 7.28 (1H, d, J=16.6 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08106064B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-54ef9bf61005419483207af4c5d88c10
Quellennotizuspto-grants-2012_01