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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15077생성일: 2026년 10월 24일

Dimethylformamide → tert-butyl (3R)-3-(2-fluoroethoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/15077

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-Fluoroethyl p-ToluenesulfonateHCID 256019—
반응물tert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl (3R)-3-(2-fluoroethoxy)pyrrolidine-1-carboxylateHCID 8661489641%

반응 단계

Sodium hydride (55% oiliness, 140 mg, 3.2 mmols) was added to DMF (5 mL) solution of tert-butyl (3R)-3-hydroxypyrrolidine-1-carboxylate (501.2 mg, 2.7 mmols) and stirred at room temperature for 30 minutes, followed by addition of 2-fluoroethyl p-toluenesulfonate (1.17 g, 5.4 mmols) and further 24 hours' stirring at the same temperature. Ethyl acetate was added to the reaction liquid which then was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the residue was purified on silica gel column chromatography (KP-Sil Sil FLASH 25+M, ethyl acetate:hexane=1:10→2:8) to provide the title compound (253 mg, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-85ad0e45c6a6422c9234ea193065d75c
출처 메모uspto-grants-2010_06