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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85127생성일: 2026년 10월 24일

1-[(3-Nitrophenyl)methyl]pyrrolidine → 3-(Pyrrolidin-1-ylmethyl)aniline

https://huagongshe.com/ko/reaction/85127

반응식

참여 물질

역할이름HCID투입량
반응물1-[(3-Nitrophenyl)methyl]pyrrolidineHCID 782880—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물3-(Pyrrolidin-1-ylmethyl)anilineHCID 109640770%

반응 단계

1-(Bromomethyl)-3-nitrobenzene (51; 5 g, 23.1 mmol) was taken up in 100 mL of anhydrous THF along with pyrrolidine (2.3 mL, 27.72 mmol) and K2CO3 (4.8 g, 34.6 mmol). The reaction mixture was stirred at room temperature for 18 h and then filtered. The filtrate was concentrated under reduced pressure to afford 1-(3-nitrobenzyl)pyrrolidine 52. This material 52 was taken up in 100 mL of absolute EtOH and 10% Pd on C (300 mg) was added. The resulting reaction mixture was stirred at room temperature under 1 atm of hydrogen for 18 h. The mixture was then filtered through a pad of Celite and the filtrate was concentrated under reduced pressure to afford 2.81 g of 3-(pyrrolidin-1-ylmethyl)aniline 53 (70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846947B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2045325230064db2aab90c3bced4e951
출처 메모uspto-grants-2014_09