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HRID 1038380作成日:2026年10月27日

2-Fluoro-5-formylbenzonitrile → 4-(3-Cyano-4-fluorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarbonitrile

https://huagongshe.com/reaction/1038380

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-5-formylbenzonitrileHCID 2769582—
反応物(2Z)-3-Amino-2-butenenitrileHCID 5325263—
溶媒Acetic AcidHCID 176—
生成物4-(3-Cyano-4-fluorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarbonitrileHCID 59763246160.7%

反応条件

温度90 °C

反応手順

30 g (201.2 mmol) 2-fluoro-5-formylbenzonitrile and 35 g (431.6 mmol) 3-aminocrotononitrile were dissolved in acetic acid (500 ml) and heated to 90° C. After 4 h, the reaction mixture was cooled to rt, concentrated, neutralized with a saturated aqueous solution of sodium bicarbonate, and extracted with ethyl acetate. The organic extracts were combined, dried over sodium sulfate and concentrated under reduced pressure. The remaining solid was dissolved in ethyl acetate, and hexane was added. The precipitate was filtered off to afford the title compound (45 g, 80% of th.) as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08551989B2
出典データセットuspto-grants-2013_10
ORD IDord-5d1dad6b490b4d95877c85768ddceb25
出典メモuspto-grants-2013_10