돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324728생성일: 2026년 10월 24일

Pyrrolidine → 1-[(3-Nitrophenyl)methyl]pyrrolidine

https://huagongshe.com/ko/reaction/324728

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물Benzene, 1-(bromomethyl)-3-nitro-HCID 77568—
용매TetrahydrofuranHCID 8028—
생성물1-[(3-Nitrophenyl)methyl]pyrrolidineHCID 782880—

반응 단계

To a solution of 3-nitrobenzylbromide (3 g, 13.9 mmol) in anhydrous THF (30 ml) was added a solution of pyrrolidine (2.3 ml, 27.8 mmol) in anhydrous THF (10 ml) dropwise with stirring. Following the addition the mixture was stirred at ambient temperature overnight. The reaction mixture was filtered, The filter cake was washed with a small volume of anhydrous THF and the filtrate was concentrated to leave the intermediate 1-(3-nitrobenzyl)pyrrolidine as an oil. This oil was dissolved in methanol (50 ml) and three equivalents of both ammonium chloride and sodium sulfide nonahydrate were added. The mixture was heated to reflux for 2 hours. After cooling the mixture was filtered. The filtercake was washed with methanol and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and dried over sodium sulfate. Filtration and evaporation of solvent left 2i quantitatively as yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218547B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-01b269a3837140e1840a894bcf157f51
출처 메모uspto-grants-2001_04