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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393572생성일: 2026년 10월 24일

N,N-Diethylaniline → 2-Hydroxy-1-naphthamide

https://huagongshe.com/ko/reaction/393572

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylanilineHCID 7061—
반응물2-Hydroxy-1-naphthoic acidHCID 16790—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매TetrahydrofuranHCID 8028—
생성물2-Hydroxy-1-naphthamideHCID 15105224345.7%

반응 조건

온도23 °C

반응 단계

Diethylaniline (0.27 μL, 1.7 μmol, 1.1 equiv) was added in one portion to a stirred solution of the amine (0.8 mg, 1.5 μmol, 1 equiv) in THF (0.2 mL) at 0° C. under an argon atmosphere and the solution was stirred for 5 min. 2-Hydroxy-1-naphthoic acid (0.37 mg, 2.0 μmol, 1.3 equiv), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.38 mg, 2.0 μmol, 1.3 equiv) and 1-hydroxybenzotriazole (0.25 mg, 1.8 μmol, 1.2 equiv) were then added separately, each in one portion, to the above solution at 0° C. The reaction mixture was warmed to 23° C. over 13 h 20 min, then was quenched with saturated aqueous ammonium chloride solution (3 mL). The mixture was diluted with ethyl acetate (10 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (10 mL) and the combined organic layer was dried over sodium sulfate. Concentration in vacuo left a white solid, which was purified by flash column chromatography (85% ethyl acetate-hexanes) to give the 2-hydroxy-naphthalene-1-carboxylic acid amide derivative (1.1 mg, 100%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809099B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-3b78a769ebff43a498e45b363e11f4fc
출처 메모uspto-grants-2004_10