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HRID 256222생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/256222

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물WaterHCID 962—
반응물ChloroselenobenzeneHCID 21928—
반응물1-Ethyl-2-oxocyclohexaneacetic Acid Methyl EsterHCID 12292028—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물6-Carbomethoxymethyl-6-ethyl-2-cyclohexen-1-oneHCID 1364924155.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04701533
출처 데이터셋uspto-grants-1987_10
ORD IDord-09a5377079f34b5099f2a44d4daee215
출처 메모uspto-grants-1987_10