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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 654519생성일: 2026년 10월 27일

Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → Methyl 1-benzylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/654519

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
반응물Borane;tetrahydrofuranHCID 2723981—
반응물Hydrochloride methanolHCID 21893726—
용매TetrahydrofuranHCID 8028—
생성물Methyl 1-benzylpyrrolidine-3-carboxylateHCID 461075150.2%

반응 단계

A solution of methyl 1-benzyl-2-oxo-4-pyrrolidylcarboxylate (D10, 35.4 g, 0.18 mole) in dry THF (135 ml) was added dropwise over 30 mins to 1M borane-THF solution (228 ml, 0.23 mole) at 0° C. under nitrogen, and when addition was complete the solution was heated under reflux for 1h. The solution was cooled to room temperature, then treated dropwise with 8% hydrogen chloride/methanol (114 ml, 0.25 mole HCl) and stirred for 18h, followed by 3h at reflux. The mixture was then concentrated in vacuo and the residue treated with water (40 ml), washed with ether (2×50 ml), basified with 40% sodium hydroxide solution, saturated with potassium carbonate and extracted with ether (3×70 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow oil, which was purified by distillation (b.p. 146° C.0.7mm) to give the title compound (D11) as a colourless oil (19.8 g, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05132316
출처 데이터셋uspto-grants-1992_07
ORD IDord-d7fce74ab2f8417f9631c77014014c0e
출처 메모uspto-grants-1992_07