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1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether

Base Information
  • Chemical Name:1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether
  • CAS No.:85382-50-9
  • Molecular Formula:C45H72F6O5SSi2
  • Molecular Weight:895.291
  • Hs Code.:
1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether

Synonyms:1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether

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Chemical Property of 1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether
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Technology Process of 1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether

There total 13 articles about 1α,3β,25-thihydroxy-26,26,26,27,27,27-hexafluorocholest-5-ene-24-yl phenyl sulfone 1,3-bis(triethylsilyl) ether 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 7 steps
2: 149 mg / pyridine / 0 °C
3: 53 percent / LiBr / dimethylformamide / 2 h / Heating
4: 92 percent / dimethylformamide / 4 h / 70 - 80 °C
5: 85 percent / 5percent KOH / methanol; tetrahydrofuran / 18 h / Ambient temperature
6: 57 percent / triethylamine / pyridine / 15 h / Ambient temperature
7: 74 percent / diisopropylamine, n-BuLi / tetrahydrofuran / 0.05 h / -78 °C
With potassium hydroxide; n-butyllithium; triethylamine; diisopropylamine; lithium bromide; In tetrahydrofuran; pyridine; methanol; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.4297
Guidance literature:
Multi-step reaction with 9 steps
1: 80 percent / 5percent NaOH, 30percent H2O2 / methanol / 18 h / Heating
2: 65 percent / lithium, anhydrous NH4Cl / liquid ammonia; tetrahydrofuran / 2 h / -78 °C
4: 149 mg / pyridine / 0 °C
5: 53 percent / LiBr / dimethylformamide / 2 h / Heating
6: 92 percent / dimethylformamide / 4 h / 70 - 80 °C
7: 85 percent / 5percent KOH / methanol; tetrahydrofuran / 18 h / Ambient temperature
8: 57 percent / triethylamine / pyridine / 15 h / Ambient temperature
9: 74 percent / diisopropylamine, n-BuLi / tetrahydrofuran / 0.05 h / -78 °C
With potassium hydroxide; sodium hydroxide; n-butyllithium; dihydrogen peroxide; lithium; ammonium chloride; triethylamine; diisopropylamine; lithium bromide; In tetrahydrofuran; pyridine; methanol; ammonia; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.4297
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