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HRID 583472Erstellt: 24. Oktober 2026

Diethyl (cyanomethyl)phosphonate → 3-(3,4-Diethylphenyl)-3-phenylacrylonitrile

https://huagongshe.com/de/reaction/583472

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl (cyanomethyl)phosphonateHCID 75676—
EduktLithium HexamethyldisilazideHCID 2733832—
EduktMethyl 3,3-bis-(3,4-dimethoxyphenyl)acrylateHCID 9820154—
Edukt3,4-DiethylbenzophenoneHCID 21584598—
LösungsmittelHexaneHCID 8058—
Produkt3-(3,4-Diethylphenyl)-3-phenylacrylonitrileHCID 54306880—

Reaktionsschritte

3-(3,4-Diethylphenyl)-3-phenylacrylonitrile was prepared analogously to methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylate using 3,4-diethylbenzophenone (0.95 g, 4 mmol), diethylcyanomethylphosphonate (0.73 mL, 4.4 mmol) and lithium hexamethyldisilazide (3.4 mL, 4.4 mmol, 1.3M) with a reaction time of 2 hours at room temperature. The crude product was purified by flash chromatography (silica gel, 8% ethyl acetate/methylene chloride) to afford an oil which was stirred in hexane until it solidified. The resulting slurry was filtered, the solid washed with hexane, air dried and then dried in vacuo to afford 0.6 g (57%) of a mixture of the E and Z isomers as a white solid: mp 63-64° C.; 1H NMR (CDCl3) δ 7.51-6.99 (m, 16H), 5.72 (s, 2H), 2.76-2.55 (m, 8H), 1.32-1.14 (m, 12H); 13C NMR (CDCl3) δ 163.3, 144.7, 142.2, 137.3, 136.5, 130.2, 129.8, 129.6, 128.6, 128.5, 128.4, 128.3, 127.2, 126.2, 118.2, 93.9, 93.7, 25.5, 25.3, 15.2, 15.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05929117
Quelldatensatzuspto-grants-1999_07
ORD IDord-43f248225c464e94bb41b7cab25611fa
Quellennotizuspto-grants-1999_07