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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385470Generated: October 26, 2026

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

https://huagongshe.com/reaction/1385470

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) δ7.51-6.99 (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) δ163.3, 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 numberUS06262101B1
Source datasetuspto-grants-2001_07
ORD IDord-9af84cd2ed844cb9a971919adf8b1468
Source noteuspto-grants-2001_07