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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7847생성일: 2026년 10월 24일

Methyl vinyl ketone → 2-Butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanone

https://huagongshe.com/ko/reaction/7847

반응식

참여 물질

역할이름HCID투입량
반응물Methyl vinyl ketoneHCID 6570—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-Butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanoneHCID 2199089281.4%

반응 단계

Methyl vinyl ketone (MVK, 0.49 mL, 5.9 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.12 mL, 0.8 mmol) were added to a solution of impure 2-butyl-5-methoxy-4-methyl-1-indanone (0.90 g, 3.9 mmol) in anhydrous tetrahydrofuran (THF, 3.9 mL). The resulting solution was stirred at room temperature for 30 hours, then diluted with Et2O (50 mL), washed with water (20 mL), 1N HCl (20 mL), and brine (20 mL), dried over MgSO4, filtered, and evaporated under vacuum to an amber oil (1.23 g). The crude product was purified by chromatography on EM silica gel 60 (230-400 mesh, 125 mL dry, packed under 4:1 hexanes-EtOAc). The column was eluted with 4:1 hexanes-EtOAc, collecting 25 mL fractions. Fractions 14-27 gave a 93:2:5 mixture (0.96 g) of 2-butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanone, the 6-methyl isomer, and the desmethyl product. This material was used in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2a4993889ca6480cb0bfdfaca22cc970
출처 메모uspto-grants-2006_08