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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29084생성일: 2026년 10월 24일

o-Methylvalerolactim → Methyl 2-[(4-fluorophenyl)-(2-methoxy-3,4,5,6-tetrahydro-pyridin-3-yl)-methyl]-4-methyl-3-oxo-pentanoate

https://huagongshe.com/ko/reaction/29084

반응식

참여 물질

역할이름HCID투입량
반응물o-MethylvalerolactimHCID 138567—
반응물Lithium diisopropylamineHCID 45051747—
반응물Methyl 2-[(4-fluorophenyl)methylidene]-4-methyl-3-oxopentanoateHCID 54501938—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-[(4-fluorophenyl)-(2-methoxy-3,4,5,6-tetrahydro-pyridin-3-yl)-methyl]-4-methyl-3-oxo-pentanoateHCID 69310350106.5%

반응 조건

온도-60 °C

반응 단계

6-Methoxy-2,3,4,5-tetrahydropyridine (102.7 g, 0.91 mole) was added over 25 min to a solution of lithium diisopropylamine (1.8 M, 505 mL, 0.91 mole) in THF (1.2 L) stirring at −60° C. under nitrogen. After stirring at −60° C. for 1 h, methyl 3-(4-fluorophenyl)-2-isobutyrylacrylate (175 g, 0.70 mole) was added over 75 min keeping the temperature below −50° C. The reaction was quenched with saturated ammonium chloride (750 mL) after the reaction had stirred at −60° C. for 35 min. After the reaction mixture had warmed to room temperature, ethyl acetate was added and the mixture transferred to a separatory funnel. The mixture was extracted with ethyl acetate (2×1 L). The combined organic layers were washed with 50% saturated ammonium chloride solution, water, and brine; dried over magnesium sulfate; and concentrated in vacuo to afford methyl 2-[(4-fluorophenyl)-(2-methoxy-3,4,5,6-tetrahydro-pyridin-3-yl)-methyl]-4-methyl-3-oxo-pentanoate (271 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420059B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1509ee9d47b9491fa2051edd8cada5c5
출처 메모uspto-grants-2008_09