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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385817Generated: October 25, 2026

4-Toluenesulfonyl chloride → HCID 17939386, compound

https://huagongshe.com/reaction/1385817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-DiiodopropaneHCID 12314—
Reactant1,4,7-TriazacyclononaneHCID 188318—
Reactant4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononaneHCID 10906262—
SolventAcetonitrileHCID 6342—
ProductHCID 17939386HCID 17939386—

Reaction Steps

1.1.19 1,3-Bis (1,4,7-triazacyclononane) propane 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-toluenesulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06264966B1
Source datasetuspto-grants-2001_07
ORD IDord-781102ef31f643c1bec493a801fd2e31
Source noteuspto-grants-2001_07