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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1007074생성일: 2026년 10월 26일

N,N,N-Tributylbutan-1-aminium trifluoroacetate → 4-[3-(3-Hydroxy-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile

https://huagongshe.com/reaction/1007074

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N-Tributylbutan-1-aminium trifluoroacetateHCID 3084618—
반응물4-[3-(3-Bromo-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrileHCID 22667595—
용매1,4-DioxaneHCID 31275—
생성물4-[3-(3-Hydroxy-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrileHCID 22667594—

반응 단계

17 g of 4-[3-(3-bromo-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrile are dissolved in 500 ml of dioxane and, after addition of 34 ml of ˜40 percent tetrabutylammonium trifluoroacetate solution, heated to reflux for 24 h. The mixture was concentrated to about half the volume, mixed with water and methyl tert-butyl ether and separated into the phases. The organic phase is concentrated, and the residue is stirred with 500 ml of ethanol and 200 ml of concentrated ammonia at room temp. for 1 h. It is then again concentrated in vacuo, and the crude product is purified on silica gel with dichloromethane/methanol =30:1 as mobile phase. The alcohol is obtained as an oil. MS (ESI): 413 (M+H+), 395 (M+H+-H2O) [C26H24N2O3 M=412].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06794359B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-a55de845b5a441349e4519abe81df536
출처 메모uspto-grants-2004_09