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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490844생성일: 2026년 10월 24일

Ammonia → 2-Hydroxy-1-naphthamide

https://huagongshe.com/ko/reaction/490844

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물2-Hydroxy-1-naphthoic acidHCID 16790—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매TetrahydrofuranHCID 8028—
생성물AmmoniaHCID 222—
생성물2-Hydroxy-1-naphthamideHCID 1510522436.8%

반응 단계

A solution of 2-hydroxy-1-napthoic acid (5.0 g, 26.6 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.6 g, 29.2 mmol), and 1-hydroxybenzotriazole (3.95 g, 29.2 mmol) in tetrahydrofuran (70 ml) was stirred at room temperature for 30 minutes prior to the addition of 0.880 NH3 (6 ml). The resulting suspension was stirred at room temperature for 2 hours. The reaction mixture was filtered and the filtrate diluted with water (80 ml) and extracted with ethyl acetate (4×80 ml). The combined organic extracts were washed with water (50 ml×2), saturated aqueous sodium chloride (50ml), dried (sodium sulfate) and the solvent removed in vacuo to give an orange oil. Purification by column chromatography on silica gel eluting with dichloromethane:methanol:0.880 ammonia 95:5:0.5 gave the title compound as a pink solid (1.83 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528170B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-9461118dbc4c4a33a4d3b548b3ab15fe
출처 메모uspto-grants-2009_05