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2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene

Base Information
  • Chemical Name:2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene
  • CAS No.:81482-25-9
  • Molecular Formula:C23H31NO6
  • Molecular Weight:417.502
  • Hs Code.:
2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene

Synonyms:2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene

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Chemical Property of 2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene
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Technology Process of 2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene

There total 8 articles about 2(2-cyano-5-ethylenedioxy-2-cyclohexylcarboxylic acid)-1,3-dimethoxy-5-pentylbenzene 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: n-BuLi
2: 87 percent / piperidine
3: 99 percent / benzene / 2 h / Heating
4: 94 percent / 6N hydrochloric acid / acetone / 0.75 h / Ambient temperature
5: 91 percent / p-toluenesulfonic acid / benzene / 2.5 h / Heating
6: 99 percent / 10percent palladium on charcoal, hydrogen / ethanol / 6 h
7: 93 percent / p-toluenesulfonic acid / benzene / 4 h / Heating
8: 94 percent / 10N aqueous sodium hydroxide / ethanol / 20 h / Heating
With piperidine; hydrogenchloride; sodium hydroxide; palladium on activated charcoal; n-butyllithium; hydrogen; toluene-4-sulfonic acid; In ethanol; acetone; benzene;
DOI:10.1139/v82-047
Guidance literature:
Multi-step reaction with 7 steps
1: 87 percent / piperidine
2: 99 percent / benzene / 2 h / Heating
3: 94 percent / 6N hydrochloric acid / acetone / 0.75 h / Ambient temperature
4: 91 percent / p-toluenesulfonic acid / benzene / 2.5 h / Heating
5: 99 percent / 10percent palladium on charcoal, hydrogen / ethanol / 6 h
6: 93 percent / p-toluenesulfonic acid / benzene / 4 h / Heating
7: 94 percent / 10N aqueous sodium hydroxide / ethanol / 20 h / Heating
With piperidine; hydrogenchloride; sodium hydroxide; palladium on activated charcoal; hydrogen; toluene-4-sulfonic acid; In ethanol; acetone; benzene;
DOI:10.1139/v82-047
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