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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583472Generated: October 25, 2026

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

https://huagongshe.com/reaction/583472

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, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929117
Source datasetuspto-grants-1999_07
ORD IDord-43f248225c464e94bb41b7cab25611fa
Source noteuspto-grants-1999_07