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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | o-Methylvalerolactim | HCID 138567 | — |
| 반응물 | Lithium diisopropylamine | HCID 45051747 | — |
| 반응물 | Methyl 2-[(4-fluorophenyl)methylidene]-4-methyl-3-oxopentanoate | HCID 54501938 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 2-[(4-fluorophenyl)-(2-methoxy-3,4,5,6-tetrahydro-pyridin-3-yl)-methyl]-4-methyl-3-oxo-pentanoate | HCID 69310350 | 106.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07420059B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-1509ee9d47b9491fa2051edd8cada5c5 |
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| 출처 메모 | uspto-grants-2008_09 |
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