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HRID 32196作成日:2026年10月23日

Sodium Iodide → 1-(2,2-Difluoroethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/ja/reaction/32196

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物2-Bromo-1,1-difluoroethaneHCID 136186—
反応物Sodium BicarbonateHCID 516892—
反応物1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物1-(2,2-Difluoroethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23141703—

反応条件

温度80 °C

反応手順

A mixture of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (30 mg, 0.1 mmol) produced in Example (8b), 2-bromo-1,1-difluoroethane (18.1 mg, 0.125 mmol), sodium iodide (1.5 mg, 0.01 mmol), potassium carbonate (20.8 mg, 0.15 mmol) and dimethylformamide (1 mL) was stirred for 2 hours at an external temperature of 80° C. After then further adding 2-bromo-1,1-difluoroethane (18.1 mg, 0.125 mmol) to the reaction mixture, it was further stirred for 6 hours and 30 minutes at an external temperature of 80° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with diethyl ether. The solvent was distilled off by nitrogen stream to the separated organic layer. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-(2,2-difluoroethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-2554bd9342da4fcd803b0ae65bebb1c8
出典メモuspto-grants-2008_09