N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine

Base Information

• Chemical Name: N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine
• CAS No.: 1283147-68-1
• Molecular Formula: C₆₉H₅₄N₄O₃
• Molecular Weight: 987.213

Synonyms:N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine

Chemical Property of N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine

Chemical Property:

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Technology Process of N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine

There total 3 articles about N₂,N₂-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N₆-(4-methoxy-phenyl)-N₆-phenylnaphthalene-2,6-diamine 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: 21.8%

N-benzyloxyamine (622-33-3) + 6-bromo-N-(4-methoxyphenyl)-N-phenylnaphthalen-2-amine (1283147-66-9) → N2,N2-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N6-(4-methoxy-phenyl)-N6-phenylnaphthalene-2,6-diamine (1283147-68-1)

Guidance literature:

With sodium t-butanolate; PtBu₃*HBF₄; palladium diacetate; In toluene; at 120 - 121 ℃; for 18h; Reflux;

Reference yield:

6-bromo-naphthalen-2-ol (15231-91-1) → N2,N2-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N6-(4-methoxy-phenyl)-N6-phenylnaphthalene-2,6-diamine (1283147-68-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: toluene-4-sulfonic acid / para-xylene / 5 h / 175 - 190 °C / Inert atmosphere; Reflux

1.2: 0.25 h / 55 °C / Reflux; Inert atmosphere

2.1: potassium hydroxide; 1,10-Phenanthroline; copper(l) chloride / toluene / 36 h / 125 °C / Inert atmosphere; Reflux

3.1: sodium t-butanolate / palladium diacetate; PtBu₃*HBF₄ / toluene / 18 h / 120 - 121 °C / Reflux

With 1,10-Phenanthroline; toluene-4-sulfonic acid; copper(l) chloride; potassium hydroxide; sodium t-butanolate; PtBu₃*HBF₄; palladium diacetate; In para-xylene; toluene;

Reference yield:

aniline (62-53-3) → N2,N2-bis(2-(N-(4-methoxyphenyl)-N-phenylamino)-naphthalen-6-yl)-N6-(4-methoxy-phenyl)-N6-phenylnaphthalene-2,6-diamine (1283147-68-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: toluene-4-sulfonic acid / para-xylene / 5 h / 175 - 190 °C / Inert atmosphere; Reflux

1.2: 0.25 h / 55 °C / Reflux; Inert atmosphere

2.1: potassium hydroxide; 1,10-Phenanthroline; copper(l) chloride / toluene / 36 h / 125 °C / Inert atmosphere; Reflux

3.1: sodium t-butanolate / palladium diacetate; PtBu₃*HBF₄ / toluene / 18 h / 120 - 121 °C / Reflux

With 1,10-Phenanthroline; toluene-4-sulfonic acid; copper(l) chloride; potassium hydroxide; sodium t-butanolate; PtBu₃*HBF₄; palladium diacetate; In para-xylene; toluene;

upstream raw materials:

aniline

6-bromo-naphthalen-2-ol

N-benzyloxyamine

6-bromo-N-(4-methoxyphenyl)-N-phenylnaphthalen-2-amine

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