1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

Base Information

• Chemical Name: 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione
• CAS No.: 121619-29-2
• Molecular Formula: C₄₄H₄₆N₄O₁₀
• Molecular Weight: 790.87
• Mol file: 121619-29-2.mol

Synonyms:1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

Chemical Property of 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

There total 3 articles about 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-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: 16.0%

5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetrahydroxy-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno[2,1,8-ija]benz[f]azulene-6,13-dione (106319-02-2) + 1,2-bis(2-chloroethoxy)ethane (112-26-5,27252-69-3) → 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione (121619-29-2)

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 70 ℃; for 48h;

DOI:10.1021/jo00276a037

Reference yield:

1,3,4,6-tatrakis(hydroxymethyl)tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione (121619-21-4) → 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione (121619-29-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 15.5 percent / p-toluenesulfonic acid monohydrate / 1,2-dichloro-ethane / 1 h / Heating

2: 16 percent / K₂CO₃ / dimethylsulfoxide / 48 h / 70 °C

With potassium carbonate; toluene-4-sulfonic acid; In dimethyl sulfoxide; 1,2-dichloro-ethane;

DOI:10.1021/jo00276a037

Reference yield:

hydroquinone (123-31-9,8027-02-9) → 1,6:3,4-bis<<3,3':6,6'-bis(1,4,7,10-tetraoxadecamethylene)>-1,2-xylylene>tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione (121619-29-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 15.5 percent / p-toluenesulfonic acid monohydrate / 1,2-dichloro-ethane / 1 h / Heating

2: 16 percent / K₂CO₃ / dimethylsulfoxide / 48 h / 70 °C

With potassium carbonate; toluene-4-sulfonic acid; In dimethyl sulfoxide; 1,2-dichloro-ethane;

DOI:10.1021/jo00276a037

upstream raw materials:

5,7,12,13b,13c,14-hexahydro-1,4,8,11-tetrahydroxy-13b,13c-diphenyl-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno[2,1,8-ija]benz[f]azulene-6,13-dione

1,2-bis(2-chloroethoxy)ethane

1,3,4,6-tatrakis(hydroxymethyl)tetrahydro-3a,6a-diphenylimidazo<4,5-d>imidazole-2,5(1H,3H)-dione

hydroquinone