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HRID 595015作成日:2026年10月24日

Triethylamine → Tert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/595015

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TetrafluoroterephthalonitrileHCID 15783—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物Tert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylateHCID 8667174351.2%

反応条件

温度55 °C

反応手順

2,3,5,6-tetrafluoroterephthalonitrile (1 g, 5 mmol) was dissolved in acetone (15 mL) in a 2-necked flask under Nitrogen. A solution of tert-butyl piperazine-1-carboxylate (1.39 g, 7.5 mmol) in water (3 mL) was then added followed by triethylamine (1.01 g, 10 mmol). The solution was heated to 55° C. for 8 h then cooled to rt. The resulting solid was filtered then washed with acetone. The filtrate was concentrated under vacuum and the residue was dissolved again in DCM (30 mL) and washed once with 1M HCl (30 mL) and once with brine (30 mL). The organics were dried over Na2SO4, filtered and the solvent removed in vacuo to give tert-butyl 4-(2,5-dicyano-3,4,6-trifluorophenyl)piperazine-1-carboxylate as a bright yellow solid (0.938 g, 51% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242987B2
出典データセットuspto-grants-2016_01
ORD IDord-0a1c2be596b64a1daf884580694e7663
出典メモuspto-grants-2016_01