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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2382186생성일: 2026년 10월 27일

Pentane → 3-(Phenyl(4-(trifluoromethyl)phenyl)methylene)piperidine

https://huagongshe.com/reaction/2382186

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물4-(Trifluoromethyl)benzophenoneHCID 69767—
반응물Tert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825—
촉매ZincHCID 23994—
촉매Titanium TetrachlorideHCID 24193—
용매TetrahydrofuranHCID 8028—
생성물3-(Phenyl(4-(trifluoromethyl)phenyl)methylene)piperidineHCID 6873458457.8%

반응 단계

To a solution of phenyl(4-(trifluoromethyl)phenyl)methanone (1.5 g, 6.0 mmol) and tert-butyl 3-oxopiperidine-1-carboxylate (1.3 g, 6.5 mmol) in THF (20 mL) was added Zn (1.8 g, 28.5 mmol) and the resulting mixture was stirred at rt for 10 min and was then cooled to 0° C. To this was added TiCl4 (1.4 mL, 13.5 mmol) dropwise. The reaction mixture was stirred first at rt for 15 min and then at 50° C. for 4 h. The solvent was removed under vacuum. Then it was cooled to 0-5° C. and added 2N HCl solution and extracted with ethyl acetate. The combined organic layer was washed with K2CO3 solution, dried over anhydrous sodium sulfate and concentrated under vacuum to afford the crude product. It was cooled to 0-5° C., pentane was added and stirred for 30 min and dried under vacuum to afford 3-(phenyl(4-(trifluoromethyl)phenyl)methylene)piperidine (1.1 g, 57% yield) as a grey solid. MS (ESI, pos. ion) m/z: 318 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08258306B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-5ac110a6a4754f578f9cad04aea3f559
출처 메모uspto-grants-2012_09