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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7851생성일: 2026년 10월 24일

1-Penten-3-one → 2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone

https://huagongshe.com/ko/reaction/7851

반응식

참여 물질

역할이름HCID투입량
반응물1-Penten-3-oneHCID 15394—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanoneHCID 21990930—

반응 조건

온도60 °C

반응 단계

A solution of 2-butyl-5-methoxy-4-methyl-1-indanone (100 mg, 0.43 mmol) in tetrahydrofuran (0.43 mL) was treated with ethyl vinyl ketone (EVK, 0.064 mL, 0.646 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.013 mL, 0.086 mmol). The resulting solution was stirred under a nitrogen atmosphere and heated in an oil bath at 60° C. After 24 hour, more EVK (0.064 mL) and DBU (0.013 mL) were added and the solution was heated an additional 24 hours at 60° C. The reaction mixture was diluted with EtOAc (10 mL) and washed with water (10 mL) containing 2N HCl (1 mL). The organic phase was washed with brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 2-butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ab9cbb76965644d483935f81bfcf3531
출처 메모uspto-grants-2006_08