돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1796206생성일: 2026년 10월 25일

m-(Trifluoromethyl)nitrobenzene → Tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1796206

반응식

참여 물질

역할이름HCID투입량
반응물m-(Trifluoromethyl)nitrobenzeneHCID 7386—
반응물TriphenylphosphineHCID 11776—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
반응물Phenol, 4-nitro-2-(trifluoromethyl)-HCID 3014014—
용매DichloromethaneHCID 6344—
용매ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
생성물Tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylateHCID 2218101888%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07030138B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-2c2b93391aae4db1b0cec91fb04f56ba
출처 메모uspto-grants-2006_04