戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 868作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物(3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl)pyrrolidineHCID 54496804—
触媒Palladium hydroxideHCID 9942167—
溶媒EthanolHCID 702—
生成物tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamateHCID 21955469—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723444
出典データセットuspto-grants-1998_03
ORD IDord-2326e4f1e4844936a51646b96ee23d0d
出典メモuspto-grants-1998_03