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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7819생성일: 2026년 10월 23일

Methyl vinyl ketone → 5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone

https://huagongshe.com/ko/reaction/7819

반응식

참여 물질

역할이름HCID투입량
반응물Methyl vinyl ketoneHCID 6570—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물5-Methoxy-2-methylindan-1-oneHCID 12290490—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanoneHCID 21990908332.6%

반응 단계

A solution of 5-methoxy-2-methyl-1-indanone (0.5 g, 2.84 mmol) in anhydrous tetrahydrofuran (3 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (0.085 mL, 0.57 mmol) and methyl vinyl ketone (0.473 mL, 5.68 mmol). The resulting solution was placed under a nitrogen atmosphere and stirred at room temperature overnight. The mixture was diluted with EtOAc (25 mL), washed with 0.2N HCl (25 mL) and brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to a yellow oil (800 mg). The oil was dissolved in CH2Cl2 (10 mL) and the solution added to a small column of EM silica gel 60 (8 mL). The column was eluted with CH2Cl2 (30 ml) and the eluant evaporated under vacuum to afford 5-methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone (467 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b2f702acf9204650b931ca10badf77fa
출처 메모uspto-grants-2006_08