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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 868생성일: 2026년 10월 23일

(3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl)pyrrolidine → tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamate

https://huagongshe.com/ko/reaction/868

반응식

참여 물질

역할이름HCID투입량
반응물(3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl)pyrrolidineHCID 54496804—
촉매Palladium hydroxideHCID 9942167—
용매EthanolHCID 702—
생성물tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamateHCID 21955469—

반응 단계

3.1 g (0.0t mol) (3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine was hydrogenated at 0.28 MPa over 0.6 g of Pearlman's catalyst (Pd(OH)2) in 40 ml ethanol (95%) over night. After filtration of the catalyst through cellite and evaporation of the solvent 1H-NMR showed that the reaction was not completed. Therefore 0.6 g of Pearlman's catalyst was added in 40 ml ethanol (95%) once more and the mixture was treated under H2 -atmosphere at 0.28 MPa over night. Filtration through cellite and evaporation of the solvent gave the product in a quantitative yield (2.18 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723444
출처 데이터셋uspto-grants-1998_03
ORD IDord-2326e4f1e4844936a51646b96ee23d0d
출처 메모uspto-grants-1998_03