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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80319생성일: 2026년 10월 24일

Pyrrolidine → 1-[Bis(4-methylphenyl)methyl]pyrrolidine

https://huagongshe.com/ko/reaction/80319

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물4,4'-DimethylbenzhydrolHCID 279356—
반응물Sodium BicarbonateHCID 516892—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
용매Thionyl ChlorideHCID 24386—
생성물1-[Bis(4-methylphenyl)methyl]pyrrolidineHCID 2514624085.5%

반응 단계

Compound 14 (0.30 g, 1.41 mmol) was dissolved in thionyl chloride (1 mL) (Wako Pure Chemical Industries, Ltd.), and the mixture was refluxed for 2 hours. The reaction solution was concentrated under reduced pressure, to thereby obtain a residue. The residue was dissolved in acetonitrile (5 mL) (Wako Pure Chemical Industries, Ltd.), and pyrrolidine (0.50 g, 7.03 mmol) was added thereto, and the mixture was refluxed for 2 hours and then allowed to cool to room temperature. A saturated aqueous solution of sodium hydrogen carbonate (Wako Pure Chemical Industries, Ltd.) was added to the reaction solution, and then mixture was extracted with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.), and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (chloroform (Wako Pure Chemical Industries, Ltd.):methanol (Wako Pure Chemical Industries, Ltd.)=99:1 as an eluent), to thereby obtain the title compound (0.32 g, 84% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846012B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-59ffcaf6c2434db88da8e3eb9c8f939f
출처 메모uspto-grants-2014_09