戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 256222作成日:2026年10月26日

Hydrogen Peroxide → 6-Carbomethoxymethyl-6-ethyl-2-cyclohexen-1-one

https://huagongshe.com/reaction/256222

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物WaterHCID 962—
反応物ChloroselenobenzeneHCID 21928—
反応物1-Ethyl-2-oxocyclohexaneacetic Acid Methyl EsterHCID 12292028—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物6-Carbomethoxymethyl-6-ethyl-2-cyclohexen-1-oneHCID 1364924155.3%

反応手順

The ketone, 2-carbomethoxymethyl-2-ethylcyclohexanone (IX) (141 mmol, 28 g) was stirred in 1.25 l of ethyl acetate (dried over 3A molecular sieves) and treated with 169 mmol (32.5 g) of PhSeCl. The reaction was stirred under nitrogen for 4 hours then treated with 250 mL of water. The mixture was shaken vigorously in a separatory funnel and the organic phase was returned to the reaction flask. Tetrahydrofuran (550 mL) was then added followed by 35 mL of 30% H2O2 (aq.) added dropwise. The reaction mixture was stirred for one hour then washed with 500 mL of water and 500 mL of saturated Na2CO3 (aq.). The product was then dried over MgSO4 and concentrated in vacuo. Flash chromatography (4 inches diameter column, 20% ethyl acetate in petroleum ether eluent, 51/2 inches of silica gel) afforded 15.3 g (78.0 mmol, 55%) of the product as a pale yellow oil. Rf =0.9 in 15% ethyl acetate/petroleum ether on TLC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04701533
出典データセットuspto-grants-1987_10
ORD IDord-09a5377079f34b5099f2a44d4daee215
出典メモuspto-grants-1987_10