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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814221Generated: November 2, 2026

Benzene → Tridecane

https://huagongshe.com/reaction/1814221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant1,4,7,10-TetraazacyclododecaneHCID 64963—
ReactantHCID 178418361HCID 178418361—
ProductTridecaneHCID 12388—

Reaction Steps

A preferred preparation of the compounds of formula IIa wherein R12 is hydrogen is to react 1,4,7,10-tetraazacyclododecane, known in the art, with dimethylformamidedimethylacetal in the presence of benzene to yield 1,4,7,10-tetraazatricyclo-[5.5,1.0]tridecane. This “tricyclic” compound is reacted with an ethanol/water mixture to yield 1-formyl-1,4,7,10-tetraazacyclododecane. This formyl compound is then reacted with t-butyl bromoacetate to yield 1-formyl-4,7,10-triscarboxymethyl-1,4,7,10-tetraazacyclododecane, tris-t-butylester. Finally, the ester groups are removed in the presence of strong acid, such as sulfuric acid, to yield a compound of formula IIa wherein R12 is hydrogen. The most preferred methods are included in Dischino, et al., Inorg. Chem., 30, 1265, 1991.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875864B2
Source datasetuspto-grants-2005_04
ORD IDord-e26908428b7e4357a6de2592e4714054
Source noteuspto-grants-2005_04