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HRID 2382186作成日:2026年10月27日

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

https://huagongshe.com/reaction/2382186

反応式

関与物質

役割名称HCID仕込み量
反応物PentaneHCID 8003—
反応物4-(Trifluoromethyl)benzophenoneHCID 69767—
反応物Tert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825—
触媒ZincHCID 23994—
触媒Titanium TetrachlorideHCID 24193—
溶媒TetrahydrofuranHCID 8028—
生成物3-(Phenyl(4-(trifluoromethyl)phenyl)methylene)piperidineHCID 6873458457.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08258306B2
出典データセットuspto-grants-2012_09
ORD IDord-5ac110a6a4754f578f9cad04aea3f559
出典メモuspto-grants-2012_09