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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974597생성일: 2026년 10월 24일

Piperidine → 1-[3-[3-(Trifluoromethyl)phenoxy]-1-azetidinylcarbonyl]piperidine

https://huagongshe.com/ko/reaction/974597

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Potassium CarbonateHCID 11430—
반응물1-Chlorocarbonyl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 19799606—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
생성물1-[3-[3-(Trifluoromethyl)phenoxy]-1-azetidinylcarbonyl]piperidineHCID 15053390—

반응 조건

온도-70 °C

반응 단계

A solution of 5.6 g (0.02 mole) of 1-chlorocarbonyl-3-[3-(trifluoromethyl)phenoxy]azetidine in 50 ml of tetrahydrofuran was treated with 3 g (0.022 mole) of potassium carbonate and while stirring, 1.9 g (0.022 mole) of piperidine was added dropwise. The mixture was then treated with 10 g of ice and stirred for 2 hr. The tetrahydrofuran was decanted then concentrated on a rotary evaporator to yield an amber oil, 6.0 g. The oil was dissolved in benzene, washed with dilute acid then water, dried over magnesium sulfate and concentrated in vacuo. This oil crystallized when cooled to -70° C. and was recrystallized from hexane with charcoal treatment at 0° C. yielding pale tan crystals, 4.5 g (68.5%), m.p. 50°-52° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05068231
출처 데이터셋uspto-grants-1991_11
ORD IDord-7b1896573f7d4ba6a0a5bb624f7954e5
출처 메모uspto-grants-1991_11