Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
m-(Trifluoromethyl)nitrobenzene → Tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | m-(Trifluoromethyl)nitrobenzene | HCID 7386 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| 반응물 | Phenol, 4-nitro-2-(trifluoromethyl)- | HCID 3014014 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 생성물 | Tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate | HCID 22181018 | 88% |
반응 단계
To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (1.45 g), 2-trifluoromethyl-4-nitrophenol (1.38 g), which was prepared from 3-trifluoromethylnitrobenzene according to the method described in J. Org. Chem., 63, 4199 (1998), and triphenylphosphine (2.27 g) in dichloromethane (65 ml), diethyl azodicarboxylate (1.4 ml) was added dropwise with stirring under ice-cooling, and the resulting mixture was stirred at room temperature overnight and then evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using dichloromethane as the eluent to afford the title compound (2.28 g, yield: 88%) as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07030138B2 |
| 출처 데이터셋 | uspto-grants-2006_04 |
| ORD ID | ord-2c2b93391aae4db1b0cec91fb04f56ba |
| 출처 메모 | uspto-grants-2006_04 |