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HRID 32155作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/32155

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-Cyclohept-1-enylphenylamineHCID 15723277—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物1-(2-Cyclohept-1-enylphenyl)piperazineHCID 2314216345.9%

反応条件

温度200 °C

反応手順

To a solution of 2-cyclohept-1-enylphenylamine (617 mg, 3.29 mmol) in 1,2-dichlorobenzene (8 mL) was added bis(2-chloroethyl)amine hydrochloride (705 mg, 3.95 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 5 hours, the reaction mixture was air-cooled to room temperature, and then 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, and then 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 387 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US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-dfb0e43c67b4425f95afc2b6765cce39
出典メモuspto-grants-2008_09