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1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester

Base Information
  • Chemical Name:1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester
  • CAS No.:83487-66-5
  • Molecular Formula:C54H44O8
  • Molecular Weight:820.939
  • Hs Code.:
1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester

Synonyms:1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester

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Chemical Property of 1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester
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Technology Process of 1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester

There total 13 articles about 1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl 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 8 steps
1: 52 percent / NaHCO3 / dimethylformamide / 1 h / 70 °C
2: 80 percent / K2CO3 / acetone / 11 h / Heating
3: 1.) n-BuLi, 2.) KOH / 1.) 0 deg C, 1 h; room temperature, overnight, 2.) MeOH, reflux, 4 h
4: 99 percent / 4-(dimethylamino)pyridine, cyclohexyl carbodiimide / CH2Cl2 / 3 h / Ambient temperature
5: 93 percent / HCl gas / benzene / 0.07 h
6: 87 percent / cupric acetate monohydrate / pyridine / 2.5 h / 40 °C
7: 66 percent / K2CO3 / acetone / 45 h / Heating
8: cupric acetate monohydrate / pyridine / 2 h / 42 °C
With hydrogenchloride; dmap; potassium hydroxide; n-butyllithium; N-cyclohexylcarbodiimide; copper diacetate; sodium hydrogencarbonate; potassium carbonate; In pyridine; dichloromethane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1021/ja00389a050
Guidance literature:
Multi-step reaction with 9 steps
1: 81 percent / KOH / 1.5 h / 250 - 300 °C
2: 52 percent / NaHCO3 / dimethylformamide / 1 h / 70 °C
3: 80 percent / K2CO3 / acetone / 11 h / Heating
4: 1.) n-BuLi, 2.) KOH / 1.) 0 deg C, 1 h; room temperature, overnight, 2.) MeOH, reflux, 4 h
5: 99 percent / 4-(dimethylamino)pyridine, cyclohexyl carbodiimide / CH2Cl2 / 3 h / Ambient temperature
6: 93 percent / HCl gas / benzene / 0.07 h
7: 87 percent / cupric acetate monohydrate / pyridine / 2.5 h / 40 °C
8: 66 percent / K2CO3 / acetone / 45 h / Heating
9: cupric acetate monohydrate / pyridine / 2 h / 42 °C
With hydrogenchloride; dmap; potassium hydroxide; n-butyllithium; N-cyclohexylcarbodiimide; copper diacetate; sodium hydrogencarbonate; potassium carbonate; In pyridine; dichloromethane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1021/ja00389a050
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