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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366632Generated: October 25, 2026

Diethyl (cyanomethyl)phosphonate → 3-(3,4-Diethylphenyl)-3-(3,4-dimethoxyphenyl)acrylonitrile

https://huagongshe.com/reaction/366632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 3,3-bis-(3,4-dimethoxyphenyl)acrylateHCID 9820154—
Reactant3',4'-Diethyl-3,4-dimethoxybenzophenoneHCID 21584604—
SolventHexaneHCID 8058—
Product3-(3,4-Diethylphenyl)-3-(3,4-dimethoxyphenyl)acrylonitrileHCID 54040106—

Reaction Steps

3-(3,4-Diethylphenyl)-3-(3,4-dimethoxyphenyl)acrylonitrile was prepared analogously to methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylate using 3',4'-diethyl-3,4-dimethoxybenzophenone (0.51 g, 1.7 mmol), diethylcyanomethylphosphonate (0.31 mL, 1.9 mmol) and lithium hexamethyldisilazide (1.4 mL, 1.9 mmol, 1.3M) with a reaction time of 60 hours at room temperature. The crude product was purified by chromatography (silica gel, 1% 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 dried in vacuo to afford 0.31 g (57%) of a mixture of the E and Z isomers as an off white solid: mp 78-82° C.; 1H NMR (CDCl3) δ 7.30-6.75 (m, 12 H), 5.61 (s, 1 H), 5.60 (s, 1 H), 3.94 (s, 3 H), 3.92 (s, 3 H), 3.87 (s, 3 H), 3.83 (s, 3 H), 2.80-2.59 (m, 8 H), 1.35-1.14 (m, 12 H); 13C NMR (CDCl3) δ 163.0, 163.0, 151.0, 150.5, 148.8, 148.6, 144.6, 143.9, 142.1, 141.8, 136.8, 134.5, 131.9, 129.7, 128.6, 128.5, 128.2, 127.3, 126.3, 123.2, 122.2, 118.7, 118.6, 112.8, 111.3, 110.7, 92.5, 92.2, 56.1, 56.0, 25.5, 25.4, 25.4, 25.3, 15.3, 15.2, 15.0, 14.9; Anal. Calcd for C21H23NO2. Theoretical: C, 78.47; H, 7.21; N, 4.36. Found: C, 77.80; H, 7.25; N, 4.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130226
Source datasetuspto-grants-2000_10
ORD IDord-0a7e5ffcd014466c99b3214b6490cfdd
Source noteuspto-grants-2000_10