(+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene

Base Information

• Chemical Name: (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene
• CAS No.: 669692-97-1
• Molecular Formula: C₄₂H₃₉N₃O₆
• Molecular Weight: 681.788

Synonyms:(+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene

Chemical Property of (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene

Chemical Property:

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Technology Process of (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene

There total 3 articles about (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene 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: 90.0%

(+/-)-2,7,12-tris(4-nitrophenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene (669692-90-4) → (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene (669692-97-1)

Guidance literature:

With hydrazine hydrate; palladium on activated charcoal; In ethanol; Heating;

DOI:10.1021/jo035557m

Reference yield:

4-Fluoronitrobenzene (350-46-9,178603-76-4) → (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene (669692-97-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 70 percent / K₂CO₃ / dimethylformamide / Heating

2: 90 percent / hydrazine hydrate / Pd/C / ethanol / Heating

With potassium carbonate; hydrazine hydrate; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;

DOI:10.1021/jo035557m

Reference yield:

cyclotriguaiacyclene (81370-49-2,68198-62-9,75322-24-6,68182-93-4) → (+/-)-2,7,12-tris(4-amino-phenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene (669692-97-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 70 percent / K₂CO₃ / dimethylformamide / Heating

2: 90 percent / hydrazine hydrate / Pd/C / ethanol / Heating

With potassium carbonate; hydrazine hydrate; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;

DOI:10.1021/jo035557m

upstream raw materials:

(+/-)-2,7,12-tris(4-nitrophenoxy)-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[adg]cyclononene

cyclotriguaiacyclene

4-Fluoronitrobenzene

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