戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4950作成日:2026年10月23日

Acetic Acid → N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethane

https://huagongshe.com/ja/reaction/4950

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物N1-(3-chlorophenyl)ethane-1,2-diamineHCID 11008376—
溶媒MethanolHCID 887—
生成物N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethaneHCID 104929773.7%

反応手順

To a stirred solution of N-(3-chlorophenyl)-1,2-diaminoethane (1 g; 0,00586 moles) in 25 ml of anhydrous methanol kept under nitrogen atmosphere, 3-quinuclidinone hydrochloride (1.01 g, 0.0062? moles) is added. The pH is adjusted to pH 6 by addition of glacial acetic acid. Sodium cyanoborohydride (0.74 g; 0.0117 moles) is added in two portions. The reaction mixture is refluxed for 10 hours, cooled and then filtered. After evaporation to dryness the residue is taken up with water, basified with 20% sodium hydroxide solution and extracted three times with ethyl acetate. The organic layer is washed with brine, dried over anhydrous sodium sulfate and, after filtration, evaporated to dryness. The residue is purified by silica gel flash-chromatography (methylene chloride--methanol--30% ammonium hydroxide, 150:50:5 as eluant) to give the desired product as a clear oil (0.06 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242929
出典データセットuspto-grants-1993_09
ORD IDord-6155d4e4a76d41d69a88452893850b2d
出典メモuspto-grants-1993_09