{N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III

Base Information

• Chemical Name: {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III
• CAS No.: 1447273-37-1
• Molecular Formula: C₃₇H₃₉IN₂NiO
• Molecular Weight: 713.324

Synonyms:{N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III

Chemical Property of {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III

Chemical Property:

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Technology Process of {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III

There total 6 articles about {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}Ni^III 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: 55.0%

bis(triphenylphosphine)nickel(II) diiodide (787624-20-8,14057-03-5) + 4,6-di-tert-butyl-2-{(trans-2-(isoindolin-2-yl)-1,2-diphenylethylimino)methyl}phenol → {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}NiIII (1447273-37-1)

Guidance literature:

4,6-di-tert-butyl-2-{(trans-2-(isoindolin-2-yl)-1,2-diphenylethylimino)methyl}phenol; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 2h;

bis(triphenylphosphine)nickel(II) diiodide; With oxygen; In tetrahydrofuran; at 20 ℃; Schlenk technique;

DOI:10.1002/ejic.201201331

Reference yield:

rac-1,2-diphenylethylene-1,2-diamine (951-87-1,5700-60-7,16635-95-3,29841-69-8,35132-20-8,107133-00-6) → {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}NiIII (1447273-37-1)

Guidance literature:

Multi-step reaction with 5 steps

1.1: tetrahydrofuran / 72 h

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 48 h / 40 °C

3.1: ethanolamine / ethanol

4.1: ethanol / 20 °C / Schlenk technique; Molecular sieve; Inert atmosphere; Reflux

5.1: sodium hydride / tetrahydrofuran / 2 h / 20 °C

5.2: 20 °C / Schlenk technique

With sodium hydride; ethanolamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 4.1: |Schiff Reaction;

DOI:10.1002/ejic.201201331

Reference yield:

1,3-dihydro-α,β-diphenyl-2H-isoindole-2-ethanamine → {N-[trans-2-(isoindolin-2-yl)-1,2-diphenylvinyl]-[3,5-bis(tert-butyl)salicylaldiminate]}NiIII (1447273-37-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: ethanol / 20 °C / Schlenk technique; Molecular sieve; Inert atmosphere; Reflux

2.1: sodium hydride / tetrahydrofuran / 2 h / 20 °C

2.2: 20 °C / Schlenk technique

With sodium hydride; In tetrahydrofuran; ethanol; 1.1: |Schiff Reaction;

DOI:10.1002/ejic.201201331

upstream raw materials:

C₂₂H₂₄N₄O₃

rac-1,2-diphenylethylene-1,2-diamine

bis(triphenylphosphine)nickel(II) diiodide

3,5-di-tert-butyl-2-hydroxybenzaldehyde

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