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6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester

Base Information
  • Chemical Name:6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester
  • CAS No.:1353640-13-7
  • Molecular Formula:C62H56O16
  • Molecular Weight:1057.12
  • Hs Code.:
6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester

Synonyms:6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester

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Chemical Property of 6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester
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Technology Process of 6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester

There total 2 articles about 6,13-dihydropentacene-2,3,9,10-tetracarboxylic acid tetrakis(3,5-bis(3,5-dimethoxy)benzyloxy)ester 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:
Guidance literature:
Multi-step reaction with 4 steps
1: tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide / 48 h / 20 °C / Reflux; Inert atmosphere
2: potassium iodide / N,N-dimethyl acetamide / 72 h / 80 °C / Inert atmosphere
3: hydrogen iodide / acetic acid; water / 48 h / Inert atmosphere; Reflux
4: lithium carbonate / N,N-dimethyl-formamide / 12 h / 70 °C / Inert atmosphere
With tetrachloromethane; N-Bromosuccinimide; hydrogen iodide; lithium carbonate; potassium iodide; dibenzoyl peroxide; In N,N-dimethyl acetamide; water; acetic acid; N,N-dimethyl-formamide; 2: |Diels-Alder Cycloaddition;
DOI:10.1246/cl.2012.1622
Guidance literature:
Multi-step reaction with 3 steps
1: potassium iodide / N,N-dimethyl acetamide / 72 h / 80 °C / Inert atmosphere
2: hydrogen iodide / acetic acid; water / 48 h / Inert atmosphere; Reflux
3: lithium carbonate / N,N-dimethyl-formamide / 12 h / 70 °C / Inert atmosphere
With hydrogen iodide; lithium carbonate; potassium iodide; In N,N-dimethyl acetamide; water; acetic acid; N,N-dimethyl-formamide; 1: |Diels-Alder Cycloaddition;
DOI:10.1246/cl.2012.1622
upstream raw materials:

dimethyl 4,5-dimethylphthalate

Downstream raw materials:

C62H54O16

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