4,4'-di-tert-butyl-4''-nitrotriphenylamine

Base Information

Chemical Name:4,4'-di-tert-butyl-4''-nitrotriphenylamine
CAS No.:1161919-44-3
Molecular Formula:C₂₆H₃₀N₂O₂
Molecular Weight:402.536
Hs Code.:

Synonyms:4,4'-di-tert-butyl-4''-nitrotriphenylamine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4,4'-di-tert-butyl-4''-nitrotriphenylamine

Chemical Property:

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Technology Process of 4,4'-di-tert-butyl-4''-nitrotriphenylamine

There total 1 articles about 4,4'-di-tert-butyl-4''-nitrotriphenylamine 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: 66.0%

: 4627-22-9
bis(4-tert-butylphenyl)amine

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 1161919-44-3
4,4'-di-tert-butyl-4''-nitrotriphenylamine

Guidance literature:: bis(4-tert-butylphenyl)amine; With sodium hydride; In dimethyl sulfoxide; mineral oil; at 20 ℃; for 0.5h;

4-Fluoronitrobenzene; In dimethyl sulfoxide; mineral oil; at 150 ℃; for 18h;

Reference yield: 80.0%

: 1161919-44-3
4,4'-di-tert-butyl-4''-nitrotriphenylamine

: 1161919-47-6
4-amino-4′,4″-di-tert-butyltriphenylamine

Guidance literature:: With palladium 10% on activated carbon; hydrazine hydrate; In ethanol; for 12h; Reflux;

Reference yield:

: 1161919-44-3
4,4'-di-tert-butyl-4''-nitrotriphenylamine

: 1609011-88-2
C₃₃H₃₄N₄O₅

Guidance literature:: Multi-step reaction with 2 steps

1: palladium on activated charcoal; hydrazine / ethanol

2: triethylamine / 1-methyl-pyrrolidin-2-one

With palladium on activated charcoal; triethylamine; hydrazine; In 1-methyl-pyrrolidin-2-one; ethanol;
DOI:10.1016/j.polymer.2014.03.031