戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1446873作成日:2026年10月27日

Dimethylformamide → methyl 2-{4-[N-methyl-N-(2-benzimidazolyl)amino]phenoxy}propionate

https://huagongshe.com/reaction/1446873

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 2-bromopropionateHCID 95576—
反応物4-[N-methyl-N-(2-benzimidazolyl)amino]phenolHCID 13314818—
溶媒WaterHCID 962—
生成物methyl 2-{4-[N-methyl-N-(2-benzimidazolyl)amino]phenoxy}propionateHCID 2055351164.5%

反応条件

温度100 °C

反応手順

A mixture of 4-[N-methyl-N-(2-benzimidazolyl)amino]phenol (1.14 g), methyl 2-bromopropionate (0.80 g), anhydrous potassium carbonate (0.72 g) and dimethylformamide (25 ml) was heated for 4 hours at a temperature of 100° C. with vigorous stirring. After cooling, the mixture was poured into water and the aqueous solution was extracted with dichloromethane. The organic extract was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The residue was purified by chromatography over silica gel with dichloromethane elution to give methyl 2-{4-[N-methyl-N-(2-benzimidazolyl)amino]phenoxy}propionate (1.0 g) as a colourless oil. The pmr spectrum of the compound was consistent with the assigned structure (CDCl3 ; chemical shift δppm): 1.50, d, 3H; 3.35, s, 3H; 3.70, s, 3H; 4.60, q, 1H; 6.50-7.60, m, 9H.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04314065
出典データセットuspto-grants-1982_02
ORD IDord-1b968bdda4ef40b1a4f561ab5ca090bc
出典メモuspto-grants-1982_02