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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375804생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydroxy-1-naphthaldehydeHCID 12819—
반응물2-CyanoethanethioamideHCID 1416277—
반응물1-(Diethylamino)ethanolHCID 15894840—
용매EthanolHCID 702—
생성물2-Cyano-3-(2-hydroxynaphth-1-yl) thioacrylamideHCID 13615347285%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05488057
출처 데이터셋uspto-grants-1996_01
ORD IDord-3668e06acc7d4dadb904439418140511
출처 메모uspto-grants-1996_01