戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1644056作成日:2026年10月27日

Ethanol → N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide

https://huagongshe.com/reaction/1644056

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Potassium HydroxideHCID 14797—
反応物1-Chloroethan-1-olHCID 12639035—
反応物4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamideHCID 57527768—
生成物N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamideHCID 5752790639%

反応条件

温度80 °C

反応手順

Potassium hydroxide (4 mmol) was dissolved in ethanol (5 mL) and heated at 80° C. 4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide (example 58) (1 mmol) was added into the solution followed by chloroethanol (3 mmol). The reaction was stirred overnight at 80° C. The reaction mixture was concentrated down and dissolved in 5% citric acid. the mixture was stirred for 1 hour. The aqueous mixture was extracted three times with ethyl acetate. The combined ethyl acetate was washed with water and dried down over sodium sulfate. The organic layer was concentrated down and purified by HPLC to yield 39% of N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide. MS (M+H, 308.25).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124121B2
出典データセットuspto-grants-2012_02
ORD IDord-a99ddfc8bf2a4c96918318e8b2828930
出典メモuspto-grants-2012_02