戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1815741作成日:2026年10月26日

4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane

https://huagongshe.com/reaction/1815741

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物Potassium CarbonateHCID 11430—
反応物1,3-DiiodopropaneHCID 12314—
反応物1,4,7-TriazacyclononaneHCID 188318—
反応物4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
溶媒AcetonitrileHCID 6342—
生成物4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
生成物HCID 17939386HCID 17939386—

反応手順

N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-bis[N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluene-sulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19). 1.1.22 1,4,7,10-Tetraazabicyclo[5.5.2]tetradecane

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06881732B2
出典データセットuspto-grants-2005_04
ORD IDord-40ea47cb16174880a641f1495dd0ae66
出典メモuspto-grants-2005_04