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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7855생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7855

반응식

참여 물질

역할이름HCID투입량
반응물1-Penten-3-oneHCID 15394—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Butyl-4-chloro-5-methoxy-1-indanoneHCID 21990917—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanoneHCID 2199091193.9%

반응 조건

온도60 °C

반응 단계

A solution of 2-butyl-4-chloro-5-methoxy-1-indanone (200 mg, 0.79 mmol) in anhydrous tetrahydrofuran (0.8 mL) was placed under a nitrogen atmosphere and treated with ethyl vinyl ketone (0.118 mL, 1.19 mmol) followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (0.024 mL, 0.158 mmol). The resulting solution was stirred and heated in an oil bath at 60° C. for 47 hours. After cooling to room temperature, the reaction mixture was diluted with EtOAc (20 mL) and washed with water (20 mL) containing 2N HCl (2 mL). The organic phase was washed with brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 2-butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone (250 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d1cb4b3435da4997860140228da64a57
출처 메모uspto-grants-2006_08