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HRID 892759作成日:2026年10月26日

Ethanol → N-(4-cyanophenyl)-4-amino-3-nitropyridine

https://huagongshe.com/reaction/892759

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物4-AminobenzonitrileHCID 13396—
反応物4-Chloro-3-nitropyridineHCID 2735781—
生成物N-(4-cyanophenyl)-4-amino-3-nitropyridineHCID 19791284—

反応手順

According to the method of J.C.S. Perkin Trans. I, 1979, 135, p-cyanoaniline (6.894 g, 58.4 mmol) was added to a solution of 4-chloro-3-nitropyridine (9.26 g, 58.4 mmol) in ethanol (200 ml) and the mixture was stirred at room temperature for 18 hours. The resulting yellow suspension was poured into 500 ml of ice-cold dilute ammonia and filtered. The solid was treated with 150 ml of boiling ethanol, cooled in ice, and filtered to give N-(4-cyanophenyl)-4-amino-3-nitropyridine, 12.15 g, as a bright yellow powder, m.p. 210°-211° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05120747
出典データセットuspto-grants-1992_06
ORD IDord-311d6e67ac3c48c49b38f8bacf7171dc
出典メモuspto-grants-1992_06