4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

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Chemical Name:4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone
CAS No.:257890-39-4
Molecular Formula:C₄₀H₄₄N₄O₈
Molecular Weight:708.811
Hs Code.:

Synonyms:4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

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Chemical Property of 4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

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Technology Process of 4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

There total 3 articles about 4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone 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: 58.0%

: 21062-20-4
diglycolyl chloride

: 75953-71-8
N,N'-diphenyl-1,5-diamino-3-oxapentane

: 257890-39-4
4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

Guidance literature:: With pyridine; In toluene; at 20 ℃;
DOI:10.1016/S0040-4020(99)00892-3

Reference yield:

: 62-53-3
aniline

: 257890-39-4
4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1: 6 h / 100 °C

2: 58 percent / pyridine / toluene / 20 °C

With pyridine; In toluene; 1: Substitution / 2: Cycloaddition;
DOI:10.1016/S0040-4020(99)00892-3

Reference yield:

: 83936-42-9
diglycolic acid dianilide

: 257890-39-4
4,10,16,22-tetraphenyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-3,11,15,23-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / LiAlH₄ / tetrahydrofuran / 6 h / Heating

2: 58 percent / pyridine / toluene / 20 °C

With pyridine; lithium aluminium tetrahydride; In tetrahydrofuran; toluene; 1: Reduction / 2: Cycloaddition;
DOI:10.1016/S0040-4020(99)00892-3