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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730165생성일: 2026년 10월 23일

N,N-Dimethylaniline → (5S)-5-(Aminomethyl)-3-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1,3-oxazolidin-2-one

https://huagongshe.com/ko/reaction/730165

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Ethyl AcetateHCID 8857—
반응물Benzyl chloroformateHCID 10387—
반응물Pyrrolidinone, (4-aminophenyl)-HCID 676146—
용매TetrahydrofuranHCID 8028—
생성물(5S)-5-(Aminomethyl)-3-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1,3-oxazolidin-2-oneHCID 11666268—

반응 조건

온도-20 °C

반응 단계

At −20° C., benzyl chloroformate (4.27 g, 25.03 mmol) is slowly added dropwise to 1-(4-aminophenyl)pyrrolidin-2-one (4 g, 22.7 mmol) and N,N-dimethylaniline (3.6 ml, 28.4 mmol) in tetrahydrofuran (107 ml). The reaction mixture is stirred at −20° C. for 30 min and then warmed to room temperature. After addition of ethyl acetate (0.5 l), the organic phase is washed with saturated NaCl solution (0.5 l). The combined organic phase are dried (magnesium sulfate), filtered and concentrated under reduced pressure. The residue is titrated with diethyl ether and filtered off with suction. Yield: 5.2 g, 74% of theory, light-beige crystals, melting point: 174° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582666B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-e3f8471f3bc24864ab0a6bc60f92aeb9
출처 메모uspto-grants-2009_09