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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561187생성일: 2026년 10월 26일

Triphenylphosphine → Tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/561187

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-TrifluoromethylphenolHCID 67958—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylateHCID 46941590—

반응 단계

To a solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (25 g, 124 mmol), 2-hydroxy-benzotrifluoride (22 g, 136 mmol) and triphenylphosphine (39 g, 149 mmol) in THF was added diethyl azodicarboxylate (23.5 mL, 149 mmol) dropwise at 0° C. The mixture was then warmed to room temperature and stirred for 14 h. The mixture was concentrated and diluted with Et2O, washed with 1 N NaOH and water and then dried over Na2SO4. The mixture was concentrated and diluted with Et2O/hexanes (35:65). The precipitated phosphine oxide was filtered and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (eluting with 35% Et2O/hexanes) to give tert-butyl 4-[2-(trifluoromethyl)phenoxy]-piperidine-1-carboxylate as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063224B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-22d4009b29a4441e9cef57dbc9ec5a72
출처 메모uspto-grants-2011_11