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HRID 579527作成日:2026年10月23日

1,2-Dichloroethane → N-methoxy-N-methyl-3-(pyridin-2-yl)propanamide

https://huagongshe.com/ja/reaction/579527

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物TriethylamineHCID 8471—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物3-(Pyridin-2-yl)propanoic acidHCID 564292—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-methoxy-N-methyl-3-(pyridin-2-yl)propanamideHCID 7898109679.3%

反応手順

A solution of 3-pyridin-2-yl-propionic acid (1.0 g, 6.62 mmol), DMAP (10 mg), and N,O-dimethylhydroxylamine hydrochloride (679 g, 7.0 mmol) and EDC (1.34 g, 7.0 mmol) in dichloromethane (40 mL) was treated with triethylamine (2.8 mL, 20.0 mmol). After stirring at room temperature overnight, the solution was poured into water, extracted with ethyl acetate (3×) and the combined organic phase was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated. Purification by column chromatography (silica gel, 30-100% ethyl acetate in heptane) gave N-methoxy-N-methyl-3-(pyridin-2-yl)propanamide (1.02 g, 78%) as a colorless oil. ESI MS found for C10H14N2O2 m/z [195.1 (M+1)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040703B2
出典データセットuspto-grants-2015_05
ORD IDord-6a376953aef548cfa575c005a815ef58
出典メモuspto-grants-2015_05