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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747908생성일: 2026년 10월 26일

Benzyl Bromide → Methyl 1-benzyl-5-oxo-2-pyrrolidinecarboxylate

https://huagongshe.com/reaction/747908

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물Methyl 5-oxo-DL-prolinateHCID 500249—
용매BenzeneHCID 241—
생성물Methyl 1-benzyl-5-oxo-2-pyrrolidinecarboxylateHCID 1109649552.6%

반응 조건

온도45 °C

반응 단계

To a slurry of NaH (22 g of 60% NaH in mineral oil, 0.55 mol) in 400 mL benzene was added the product of Example 1A (0.387 mol) in 100 mL benzene dropwise via addition funnel. The mixture stirred for 30 minutes after the addition was complete, then was warmed to reflux and allowed to stir for 1.5 h. The reaction was cooled to 45° C. and stirred for 16 h. A portion of benzyl bromide (45 mL, 0.38 mol) was added, the mixture was warmed to reflux and an additional amount of benzyl bromide was added (45 mL, 0.38 mol). This solution stirred for 24 h at reflux, then was cooled to ambient temperature, filtered through Celite® diatomaceous earth and the residue was washed with CH2Cl2. The combined filtrates were concentrated under reduced pressure and excess benzyl bromide was removed via distillation. The distillation residue was purified via column chromatography (SiO2, 75% hexanes-EtOAc) to give 46.6 g of the title compound (0.2 mol, 52% yield). MS (DCl/NH3) m/z 234 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399765B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-610e2f2cde104440b7d7bb4454edf400
출처 메모uspto-grants-2008_07