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HRID 375804作成日:2026年10月24日

2-Hydroxy-1-naphthaldehyde → 2-Cyano-3-(2-hydroxynaphth-1-yl) thioacrylamide

https://huagongshe.com/ja/reaction/375804

反応式

関与物質

役割名称HCID仕込み量
反応物2-Hydroxy-1-naphthaldehydeHCID 12819—
反応物2-CyanoethanethioamideHCID 1416277—
反応物1-(Diethylamino)ethanolHCID 15894840—
溶媒EthanolHCID 702—
生成物2-Cyano-3-(2-hydroxynaphth-1-yl) thioacrylamideHCID 13615347285%

反応手順

A mixture of 2-hydroxy-1-naphthaldehyde (172 mg, 1 mmol), 2-cyanothioacetamide (110 mg, 1.1 mmol), N,N-diethylaminoethanol (23 mg, 0.2 mmol) and 15 ml ethanol is stirred for 30 min at reflux under nitrogen. Then the mixture is chilled, the precipitate filtered, washed with ice-cooled ethanol and dried in a vacuum-oven. Thus an almost pure title compound is obtained in 85% yield (1080 mg). Recrystallization from ethanol furnishes very pure samples.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05488057
出典データセットuspto-grants-1996_01
ORD IDord-3668e06acc7d4dadb904439418140511
出典メモuspto-grants-1996_01