戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 48133作成日:2026年10月24日

Water → 2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile

https://huagongshe.com/ja/reaction/48133

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-Hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 86759358—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 5452275141%

反応条件

温度0 °C

反応手順

2-hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.8 g; 9 mmol) is dissolved in 15 ml of anhydrous tetrahydrofuran, and cooled to 0° C. Methanesulfonyl chloride (0.93 ml, 0.012 mol) is added at once, followed by triethylamine (2 ml, 0.015 mol) dropwise over 20 min, keeping the temperature of the mixture below 5° C. The mixture is then stirred at 2° C. for 1 h 15 min, and poured into 200 ml of iced water. The suspension is extracted with ethyl acetate, the organic extract is washed neutral with water, then with brine, and dried over magnesium sulfate. Rotary evaporation of the solvent and recrystallization from 80 ml of ethanol yields 2-methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.02 g; 41%) as light yellow hair-like crystals, mp 147-152° C. (dec). 1H-NMR reveals the presence of only one isomer.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703182B1
出典データセットuspto-grants-2004_03
ORD IDord-212d808d04a24f93b79c9b42fc64dcf5
出典メモuspto-grants-2004_03