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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1815741Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1815741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktPotassium CarbonateHCID 11430—
Edukt1,3-DiiodopropaneHCID 12314—
Edukt1,4,7-TriazacyclononaneHCID 188318—
Edukt4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
LösungsmittelAcetonitrileHCID 6342—
Produkt4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
ProduktHCID 17939386HCID 17939386—

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06881732B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-40ea47cb16174880a641f1495dd0ae66
Quellennotizuspto-grants-2005_04