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HRID 426166作成日:2026年10月24日

Benzaldehyde, 3,5-dimethyl- → 3-(3,5-Dimethyl-phenyl)-acrylonitrile

https://huagongshe.com/ja/reaction/426166

反応式

関与物質

役割名称HCID仕込み量
反応物Benzaldehyde, 3,5-dimethyl-HCID 34225—
反応物Diethyl (cyanomethyl)phosphonateHCID 75676—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3,5-Dimethyl-phenyl)-acrylonitrileHCID 6670545394.3%

反応手順

To a stirred mixture of 3,5-dimethyl benzaldehyde (13.4 g, 0.1M), diethyl cyanomethylphosphonate (19.4 g, 0.11M) in anhydrous THF (200 ml) under nitrogen at 0° C. (ice bath), was added potassium t-butoxide (12.3 g, 0.11M). After stirring for 1 hr., the mixture was stirred for overnight at room temperature. The mixture was then partitioned between ether and water. The ether layer was taken, dried with anhydrous magnesium sulfate, filtered, evaporated in vacuo, and the residue was purified by silica gel column chromatography (eluent, ether:hexanes (1:20)) to afford 14.8 g (86%) of a white solid. m.p. 67-68° C.; 1H NMR (200 MHz, CDCl3) δ 2.33 (6H, s), 5.83 (1H, d, J=16.6 Hz), 7.05 (3H, s), 7.28 (1H, d, J=16.6 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08106064B2
出典データセットuspto-grants-2012_01
ORD IDord-54ef9bf61005419483207af4c5d88c10
出典メモuspto-grants-2012_01