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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499733생성일: 2026년 10월 26일

N,N-Dimethylaniline → Benzyl 4-(2-oxo-1-pyrrolidinyl)phenylcarbamate

https://huagongshe.com/reaction/499733

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Ethyl AcetateHCID 8857—
반응물Benzyl chloroformateHCID 10387—
반응물Pyrrolidinone, (4-aminophenyl)-HCID 676146—
용매TetrahydrofuranHCID 8028—
생성물Benzyl 4-(2-oxo-1-pyrrolidinyl)phenylcarbamateHCID 768649673.8%

반응 조건

온도-20 °C

반응 단계

4.27 g (25.03 mmol) of benzyl chloroformate are slowly added to 4 g (22.7 mmol) of 1-(4-aminophenyl)pyrrolidin-2-one and 3.6 ml (28.4 mmol) of N,N-dimethylaniline in 107 ml of tetrahydrofuran at −20° C. The mixture is stirred at −20° C. for 30 minutes and then allowed to reach room temperature. 0.5 l of ethyl acetate is added, and the organic phase is washed with 0.5 l of saturated NaCl solution. The removed organic phase is dried with MgSO4, and the solvent is evaporated in vacuo. The residue is triturated with diethyl ether and filtered off with suction. 5.2 g (73.8% of theory) of benzyl 4-(2-oxo-1-pyrrolidinyl)phenylcarbamate are obtained as pale beige crystals with a melting point of 174° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767702B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-b678ad7d47524d1ab57465d1e6ea7d61
출처 메모uspto-grants-2010_08