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2-Cyclopenten-1-one, 3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth yl-

Base Information
  • Chemical Name:2-Cyclopenten-1-one, 3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth yl-
  • CAS No.:596122-07-5
  • Molecular Formula:C21H28O4S
  • Molecular Weight:376.517
  • Hs Code.:
2-Cyclopenten-1-one,
3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth
yl-

Synonyms:

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Chemical Property of 2-Cyclopenten-1-one, 3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth yl-
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Technology Process of 2-Cyclopenten-1-one, 3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth yl-

There total 7 articles about 2-Cyclopenten-1-one, 3-ethoxy-5-[(3E)-5-hydroxy-4-methyl-6-(phenylsulfinyl)-3-hexenyl]-5-meth yl- 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:
racemic methyl phenyl sulfoxide; With n-butyllithium; diisopropylamine; In tetrahydrofuran; at -78 ℃; for 0.5h;
5-(4-ethoxy-1-methyl-2-oxocyclopent-3-enyl)-2-methylpent-2-enal; In tetrahydrofuran; at -78 ℃; for 1h;
DOI:10.1021/jo034280n
Guidance literature:
Multi-step reaction with 7 steps
1.1: n-BuLi; diisopropylamine / tetrahydrofuran / 0.5 h / -78 °C
1.2: 60 percent / tetrahydrofuran / 3 h / -78 °C
2.1: KH / dimethylformamide / 0.17 h / 20 °C
2.2: 77 percent / dimethylformamide / 3 h
3.1: 74 percent / KOH / ethanol / 16 h / Heating
4.1: n-BuLi; diisopropylamine / tetrahydrofuran / 0.5 h / -78 °C
4.2: 81 percent / tetrahydrofuran / 3 h / -78 °C
5.1: Sudan Red 23; ozone / CH2Cl2; methanol / 0.08 h / -78 °C
5.2: 90 percent / PPh3 / CH2Cl2; methanol / -78 - 20 °C
6.1: 293 mg / benzene / 10 h / Heating
7.1: n-BuLi; diisopropylamine / tetrahydrofuran / 0.5 h / -78 °C
7.2: 55 percent / tetrahydrofuran / 1 h / -78 °C
With potassium hydroxide; n-butyllithium; potassium hydride; ozone; diisopropylamine; Sudan III; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; benzene; 6.1: Wittig reaction;
DOI:10.1021/jo034280n
Guidance literature:
Multi-step reaction with 6 steps
1.1: KH / dimethylformamide / 0.17 h / 20 °C
1.2: 77 percent / dimethylformamide / 3 h
2.1: 74 percent / KOH / ethanol / 16 h / Heating
3.1: n-BuLi; diisopropylamine / tetrahydrofuran / 0.5 h / -78 °C
3.2: 81 percent / tetrahydrofuran / 3 h / -78 °C
4.1: Sudan Red 23; ozone / CH2Cl2; methanol / 0.08 h / -78 °C
4.2: 90 percent / PPh3 / CH2Cl2; methanol / -78 - 20 °C
5.1: 293 mg / benzene / 10 h / Heating
6.1: n-BuLi; diisopropylamine / tetrahydrofuran / 0.5 h / -78 °C
6.2: 55 percent / tetrahydrofuran / 1 h / -78 °C
With potassium hydroxide; n-butyllithium; potassium hydride; ozone; diisopropylamine; Sudan III; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; benzene; 5.1: Wittig reaction;
DOI:10.1021/jo034280n
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