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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366630Generated: October 25, 2026

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

https://huagongshe.com/reaction/366630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 3,3-bis-(3,4-dimethoxyphenyl)acrylateHCID 9820154—
Reactant3,4-DiethylbenzophenoneHCID 21584598—
SolventHexaneHCID 8058—
Product3-(3,4-Diethylphenyl)-3-phenylacrylonitrileHCID 54306880—

Reaction Steps

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, 16 H), 5.72 (s, 2 H), 2.76-2.55 (m, 8 H), 1.32-1.14 (m, 12 H); 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130226
Source datasetuspto-grants-2000_10
ORD IDord-2f971f3528ee4d93a5e1f2583d38984f
Source noteuspto-grants-2000_10