7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

Base Information

Chemical Name:7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane
CAS No.:87497-84-5
Molecular Formula:C₂₂H₁₉N₃O₄
Molecular Weight:389.411
Hs Code.:

7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0<sup>1,5</sup>>undecane

Synonyms:7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

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Chemical Property of 7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

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Technology Process of 7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

There total 4 articles about 7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

: 87497-81-2,99121-63-8
2,5-dibenzyl-3a,6a-dicarbamoyl-1,4-dioxo-octahydropyrrolo<3,4-c>pyrrole

: 87497-84-5
7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

Guidance literature:: at 235 - 240 ℃; for 1.25h;

Reference yield:

: 632-56-4
tetraethyl ethane-1,1,2,2-tetracarboxylate

: 87497-84-5
7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

Guidance literature:: Multi-step reaction with 3 steps

1: 83.5 percent / trifluoroacetic acid / 100 °C

2: 58.5 percent / ammonia / ethanol / 72 h / 100 °C

3: 78 percent / 1.25 h / 235 - 240 °C

With ammonia; trifluoroacetic acid; In ethanol;

Reference yield:

: 2547-66-2
1,3,5-Tribenzyl-1,3,5-triazacyclohexane

: 87497-84-5
7,10-dibenzyl-2,4,6,9-tetraoxo-3,7,10-triazatricyclo<3.3.3.0^1,5>undecane

Guidance literature:: Multi-step reaction with 3 steps

1: 83.5 percent / trifluoroacetic acid / 100 °C

2: 58.5 percent / ammonia / ethanol / 72 h / 100 °C

3: 78 percent / 1.25 h / 235 - 240 °C

With ammonia; trifluoroacetic acid; In ethanol;