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HRID 2218803作成日:2026年10月27日

Bis(2-chloroethyl)amine hydrochloride → 1-(2-Cyclooct-1-enylphenyl)piperazine

https://huagongshe.com/reaction/2218803

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-chloroethyl)amine hydrochlorideHCID 522769—
反応物2-Cyclooct-1-enylphenylamineHCID 53987901—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物1-(2-Cyclooct-1-enylphenyl)piperazineHCID 6921898253.2%

反応条件

温度200 °C

反応手順

To a solution of 2-cyclooct-1-enylphenylamine (140 mg, 0.695 mmol) in 1,2-dichlorobenzene (2 mL) was added bis(2-chloroethyl)amine hydrochloride (149 mg, 0.835 mmol), and the mixture was stirred at an external temperature of 200° C. under a nitrogen atmosphere. During the reaction, a nitrogen stream was blown into the reactor to remove the hydrogen chloride gas in the reactor. This procedure was repeated several times. After 9 hours, the mixture was air-cooled to room temperature. Aqueous solution of potassium carbonate, ethyl acetate and methanol were added to the reaction mixture and extraction was performed three times with ethyl acetate. The obtained organic layers were dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 100 mg of the title compound as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07410971B2
出典データセットuspto-grants-2008_08
ORD IDord-f0a9864d89a849849b25cc56c19bc9ad
出典メモuspto-grants-2008_08