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HRID 490844作成日:2026年10月25日

Ammonia → 2-Hydroxy-1-naphthamide

https://huagongshe.com/reaction/490844

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物2-Hydroxy-1-naphthoic acidHCID 16790—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒TetrahydrofuranHCID 8028—
生成物AmmoniaHCID 222—
生成物2-Hydroxy-1-naphthamideHCID 1510522436.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528170B2
出典データセットuspto-grants-2009_05
ORD IDord-9461118dbc4c4a33a4d3b548b3ab15fe
出典メモuspto-grants-2009_05