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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354432생성일: 2026년 10월 24일

Boc-L-Pro-Ome → 1-tert-Butyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate

https://huagongshe.com/ko/reaction/354432

반응식

참여 물질

역할이름HCID투입량
반응물Boc-L-Pro-OmeHCID 1277666—
반응물Cornforth reagentHCID 2724130—
용매DichloromethaneHCID 6344—
생성물1-tert-Butyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylateHCID 425185357%

반응 단계

To a stirred solution of N-Boc proline methyl ester (2 .0 g, 8.15 mmol) in CH2Cl2 were added 3 A molecular sieves (2 g) and PDC (4.60 g, 12.2 mmol). The mixture was stirred for 3 days. The mixture was filtered through a Celiete pad and the filtrate was evaporated. The residue was chromatographed on silica gel with CHCl3—MeOH (10:1) as eluent to give methyl 1-(tert-butoxycarbonyl)-4-oxopyrrolidine-2-carboxylate (1.13 g, 57%) as a colorless oil. 1H-NMR (CDCl3) δ1.46-1.48 (m, 9 H), 2.56-2.61 (m, 1 H), 2.88-3.00 (m, 1 H), 3.77 (s, 3 H), 3.82-3.88 (m, 2 H), 4.71-4.83 (m, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756378B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-aa8445ab165f4ab9946713dfe11e1ed1
출처 메모uspto-grants-2004_06