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HRID 260795作成日:2026年10月26日

4-Aminobenzonitrile → 4-[(2-Ethoxy-3,4-dioxocyclobut-1-en-1-yl)amino]benzonitrile

https://huagongshe.com/reaction/260795

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminobenzonitrileHCID 13396—
反応物Diethyl squarateHCID 123228—
溶媒EthanolHCID 702—
生成物4-[(2-Ethoxy-3,4-dioxocyclobut-1-en-1-yl)amino]benzonitrileHCID 10824058—

反応手順

4-Aminobenzonitrile (17.58 g, 149 mmol) was added to a solution of 3,4-diethoxy-3-cyclobutene-1,2-dione (25.31 g, 149 mmol) in absolute ethanol (450 mL). The mixture was heated at reflux overnight and the resulting suspension filtered hot to remove a small amount of a dirty yellow solid (discarded). The tiltrate was gradually concentrated to afford several crops of 4-(3,4-dioxo-2-ethoxy-cyclobut-1-enylamino)-benzonitrile, as a bright yellow solid, which were collected by filtration and combined. Yield: 29.11 g (81%): 1H NMR (DMSO-d6): δ 11.07 (s, 1H), 7.81 (d, 2H), 7.56 (d, 2H), 4.79 (q, 2H), 1.46 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05530025
出典データセットuspto-grants-1996_06
ORD IDord-df06eb08e0e64101b8733fed77b72d36
出典メモuspto-grants-1996_06