(2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione

Base Information

• Chemical Name: (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione
• CAS No.: 78049-88-4
• Molecular Formula: C₁₅H₆Br₆N₂O₄
• Molecular Weight: 757.648

Synonyms:(2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione

Chemical Property of (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione

Chemical Property:

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Technology Process of (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione

There total 5 articles about (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione 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: 89.0%

N-(4-nitrophenyl)maleimide (4338-06-1) + hexabromocyclopenta-1,3-diene (14310-17-9) → (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (78049-88-4)

Guidance literature:

In chlorobenzene; at 130 ℃; for 10h;

Reference yield:

(2R,3S)-1,4,5,6,7,7-Hexabromo-3-(4-nitro-phenylcarbamoyl)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (78049-98-6) → (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (78049-88-4)

Guidance literature:

at 200 - 210 ℃; for 2h; Yield given;

Reference yield:

4-nitro-aniline (100-01-6,104810-17-5) → (2S,6R)-1,7,8,9,10,10-Hexabromo-4-(4-nitro-phenyl)-4-aza-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (78049-88-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / acetone

2: 2 h / 200 - 210 °C

In acetone;

upstream raw materials:

N-(4-nitrophenyl)maleimide

hexabromocyclopenta-1,3-diene

(2R,3S)-1,4,5,6,7,7-Hexabromo-3-(4-nitro-phenylcarbamoyl)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

4-nitro-aniline

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