戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 567216作成日:2026年10月26日

Dimethyl Sulfoxide → 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-one

https://huagongshe.com/reaction/567216

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Hydrogen PeroxideHCID 784—
反応物1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidineHCID 98642—
溶媒WaterHCID 962—
生成物1-Methoxy-2,2,6,6-tetramethylpiperidin-4-oneHCID 1097619378%

反応条件

温度30.5 °C

反応手順

A 5.0 L 4 neck mechanically stirred flask is charged with 1oxyl-2,2,6,6-tetramethyl-4-piperidone (300 g, 1.76 moles), ferrous sulfate heptahydrate (513.7 g, 1.85 moles) and dimethylsulfoxide (1450 g). Hydrogen peroxide, 30% (279.2 g, 2.46 moles), is added over a 1 hour 45 min span. The temperature is maintained at 29-32° C. The content is stirred for an additional 30 min at 25-30° C. and then chilled below 1° C. Water (1250 ml) is added and the mixture is extracted with four 750 ml portions of ethyl acetate. The combined extracts are washed, 2×1.0 L of H2O, then 1×500 ml of saturated NaCl and then dried over anhydrous MgSO4. Ethyl acetate is evaporated and the product is distilled (82-84° C. 10.33×10−2 bar), yielding 254 g of a pale yellow oil (yield: 78% of theory; IR-spectrum: Ketone carbonyl, 1710 cm-1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06177491B1
出典データセットuspto-grants-2001_01
ORD IDord-a96b15b85c9246918e9ffc9db6f74dc4
出典メモuspto-grants-2001_01