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1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP

Base Information
  • Chemical Name:1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP
  • CAS No.:95233-98-0
  • Molecular Formula:C23H30O6
  • Molecular Weight:402.488
  • Hs Code.:
1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP

Synonyms:1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP

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Chemical Property of 1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP
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Technology Process of 1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP

There total 11 articles about 1,2-cis-2,3-trans-3,4-trans-2-(2-propen-1-yl)-3-ethoxycarbonyl-cyclopentan-4-benzoyloxy-1-ol-1-THP 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 9 steps
1: 50 percent / K2CO3 / dimethylformamide / Ambient temperature
2: 97 percent / n-butyllithium, diisopropylamide, / hexane; tetrahydrofuran / 1 h / Ambient temperature
3: 70 percent / p-toluenesulfonic acid / benzene / Heating
4: 50percent sulfuric acid, silica gel / CH2Cl2 / 5 h / Ambient temperature
5: 70 percent / K-Selectride / tetrahydrofuran / 4 h / -78 °C
6: 94 percent / sulfuric acid, silica gel / CH2Cl2 / 30 h
7: PPTS / CH2Cl2 / 4 h / Ambient temperature
8: 93 percent / NaBH4 / ethanol; H2O / 1 h / 0 °C
9: 85 percent / triethylamine, DMAP / CH2Cl2 / 1.5 h / 0 °C
With dmap; sodium tetrahydroborate; n-butyllithium; sulfuric acid; pyridinium p-toluenesulfonate; silica gel; potassium tri-sec-butyl-borohydride; potassium carbonate; triethylamine; diisopropylamine; toluene-4-sulfonic acid; In tetrahydrofuran; ethanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1016/S0040-4020(01)91299-2
Guidance literature:
Multi-step reaction with 9 steps
1: 50 percent / K2CO3 / dimethylformamide / Ambient temperature
2: 97 percent / n-butyllithium, diisopropylamide, / hexane; tetrahydrofuran / 1 h / Ambient temperature
3: 70 percent / p-toluenesulfonic acid / benzene / Heating
4: 50percent sulfuric acid, silica gel / CH2Cl2 / 5 h / Ambient temperature
5: 70 percent / K-Selectride / tetrahydrofuran / 4 h / -78 °C
6: 94 percent / sulfuric acid, silica gel / CH2Cl2 / 30 h
7: PPTS / CH2Cl2 / 4 h / Ambient temperature
8: 93 percent / NaBH4 / ethanol; H2O / 1 h / 0 °C
9: 85 percent / triethylamine, DMAP / CH2Cl2 / 1.5 h / 0 °C
With dmap; sodium tetrahydroborate; n-butyllithium; sulfuric acid; pyridinium p-toluenesulfonate; silica gel; potassium tri-sec-butyl-borohydride; potassium carbonate; triethylamine; diisopropylamine; toluene-4-sulfonic acid; In tetrahydrofuran; ethanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1016/S0040-4020(01)91299-2
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