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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242559생성일: 2026년 10월 24일

Methyl iodide → 1-Benzyl-3,5-dimethylpiperidin-4-one

https://huagongshe.com/ko/reaction/242559

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물1-Benzyl-3-methyl-4-piperidoneHCID 560965—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-3,5-dimethylpiperidin-4-oneHCID 22278920—

반응 조건

온도-78 °C

반응 단계

To 1-benzyl-3-methyl-4-piperidone (2.0 g, 9.8 mmol) in THF at about −78° C. under argon, was added Lithium diisopropylamide (7.35 mL, 14.7 mmol, 2 M in heptane/THF/ethylbenzene). After stirring for about 1 hour at about −78° C., iodomethane (0.73 mL, 11.8 mmol) was added. The reaction mixture was stirred for about 1 hour at about −78° C., then warmed to room temperature. Stirring was continued overnight at room temperature. The reaction was quenched with saturated ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with water, then brine and dried over magnesium sulfate. The crude product was chromatographed on silica gel, eluting with EtOAc/hexane (3:10) to give a yellow oil of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653096B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d139616e329d44ceabb8a5c420ff567d
출처 메모uspto-grants-2014_02