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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423392생성일: 2026년 10월 25일

1,1'-Carbonyldiimidazole → Tert-butyl 3-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/423392

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acidHCID 2760529—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 3-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylateHCID 5741960590%

반응 단계

Add in one portion 1,1′-carbonyldiimidazole (8.3 g, 51 mmol) to a solution of pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester (10.0 g, 46.5 mmol) in dichloromethane (155 mL) at RT. Allow the mixture to stir for 15 min. Add slowly N,O-dimethylhydroxylamine hydrochloride (5.4 g, 55.8 mmol). Stir the reaction mixture at RT overnight. Dilute the mixture with dichloromethane (200 mL), wash with water (2×300 mL), brine (200 mL), dry over Na2SO4, filter, and concentrate. Purify the crude material by flash chromatograph and elute with 50-100% ethylacetate/hexane to give 10.8 g (90%) of the title compound. LC-MS/ES m/z 203.0 [M-tert-Bu+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101764B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-5a2427e5e4d943378acb9ddb6e26de1e
출처 메모uspto-grants-2012_01