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HRID 583472作成日:2026年10月26日

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

https://huagongshe.com/reaction/583472

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (cyanomethyl)phosphonateHCID 75676—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylateHCID 9820154—
反応物3,4-DiethylbenzophenoneHCID 21584598—
溶媒HexaneHCID 8058—
生成物3-(3,4-Diethylphenyl)-3-phenylacrylonitrileHCID 54306880—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929117
出典データセットuspto-grants-1999_07
ORD IDord-43f248225c464e94bb41b7cab25611fa
出典メモuspto-grants-1999_07