Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N,N,N-Tributylbutan-1-aminium trifluoroacetate → 4-[3-(3-Hydroxy-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N,N,N-Tributylbutan-1-aminium trifluoroacetate | HCID 3084618 | — |
| 반응물 | 4-[3-(3-Bromo-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrile | HCID 22667595 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-[3-(3-Hydroxy-3-phenylpropyl)-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06794359B2 |
| 출처 데이터셋 | uspto-grants-2004_09 |
| ORD ID | ord-a55de845b5a441349e4519abe81df536 |
| 출처 메모 | uspto-grants-2004_09 |