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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640967생성일: 2026년 10월 25일

Potassium Carbonate → 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidine

https://huagongshe.com/reaction/640967

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
반응물3-Fluoro-pyrrolidine dihydrochloride saltHCID 68700533—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidineHCID 68699478—

반응 조건

온도50 °C

반응 단계

A solution of 3-Fluoro-pyrrolidine dihydrochloride salt (448 mg, 3.584 mmol) in anhydrous acetonitrile (24 mL) was treated with bromopropoxy-tert-butyldimethyl silane (0.83 mL) and then with K2CO3 (2.5 g, 5 equiv.). The reaction mixture was heated to 50° C. and stirred overnight. The reaction mixture was subsequently diluted with water (75 mL) and extracted with a 6:1 mixture of Hexane and diethyl ether (2×100 mL). The organic layer was washed with NaHCO3(aq) (100 mL) and brine (100 mL) then dried over anhydrous K2CO3. Following filtration and concentration of the filtrate in vacuo the crude product was purified by flash silica gel chromatography (MeOH:EtOAc, 1:20). By 1H NMR the resulting clear oil (0.8 g) was the desired 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidine in a 10:1 ratio with the t-butyldimethylsilanol by-product. This residue was carried on without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07692005B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-b141d4638d294d85a0a0a2508f31772e
출처 메모uspto-grants-2010_04