돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1353059생성일: 2026년 10월 24일

Sodium hydride → 1-(2-(2-Methoxy-4-nitrophenoxy)ethyl)pyrrolidine

https://huagongshe.com/ko/reaction/1353059

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-5-nitroanisoleHCID 70519—
반응물1-PyrrolidineethanolHCID 76288—
용매DimethylformamideHCID 6228—
생성물1-(2-(2-Methoxy-4-nitrophenoxy)ethyl)pyrrolidineHCID 17989355—

반응 단계

To a solution of the 1-(2-hydroxyethyl)-pyrrolidine [Aldrich], (1.87 ml, 16 mmol) in dimethylformamide was added portionwise sodium hydride [60% dispersion in oil, (544 mg, 16 mmol). After stirring at room temperature for 10 minutes a solution of 1-chloro-2-methoxy-4-nitro-benzene [Avocado] (3 g, 16 mmol) in dimethylformamide (10 ml) was added dropwise. The reaction mixture was left stirring at room temperature for 16 hrs then concentrated. The residue was dissolved in ethyl acetate (200 ml) and washed with water (3×50 ml). The organic phase was dried with magnesium sulphate, evaporated and the residue purified by flash chromatography on silica gel using dichloromethane-aq. ammonia-methanol as eluent to afford 1-[2-(2-methoxy-4-nitro-phenoxy)-ethyl]-pyrrolidine as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220777B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-e055248d058841af828214408c0156d1
출처 메모uspto-grants-2007_05