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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899753Generated: October 31, 2026

Benzene → Tridecane

https://huagongshe.com/reaction/1899753

Reaction equation

Participants

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

Reaction Steps

A preferred method for the preparation of the compounds of formula IIa wherein R14 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 R14 is hydrogen. The most preferred methods for the preparation of formula IIa compounds are included in Dischino, et al., Inorg. Chem,, 30, 1265, 1991.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05573752
Source datasetuspto-grants-1996_11
ORD IDord-8e689ef3eba04319b446082749c87cc4
Source noteuspto-grants-1996_11