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3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane

Base Information Edit
  • Chemical Name:3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane
  • CAS No.:1359697-41-8
  • Molecular Formula:C31H45IO5
  • Molecular Weight:624.6
  • Hs Code.:
  • Mol file:1359697-41-8.mol
3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane

Synonyms:3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane

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Chemical Property of 3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane Edit
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Technology Process of 3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane

There total 6 articles about 3α,16α,24-trihydroxy-7α-(3'-iodobenozyl)oxy-5β-cholane 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:
methyl Δ-16-3α-acetoxy-7α-(3'-iodobenzoyl)oxy-5β-cholan-24-oate; With borane-THF; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; water; at 0 ℃; for 3h;
With potassium carbonate; In methanol; at 20 ℃; for 2h;
DOI:10.1021/ml200256d
Guidance literature:
Multi-step reaction with 6 steps
1.1: toluene-4-sulfonic acid / 2 h / Sonication
2.1: sodium hydrogencarbonate / tetrahydrofuran / Reflux
3.1: calcium hydride; N-benzyl-N,N,N-triethylammonium chloride / toluene / 48 h / Reflux
4.1: (Dichloroiodo)benzene; tert-butyl alcohol / dichloromethane / 1 h / 0 °C / Photolysis; Inert atmosphere
5.1: pyridine / Reflux
6.1: borane-THF / tetrahydrofuran / 2 h / 0 - 20 °C
6.2: 3 h / 0 °C
6.3: 2 h / 20 °C
With pyridine; calcium hydride; borane-THF; (Dichloroiodo)benzene; N-benzyl-N,N,N-triethylammonium chloride; sodium hydrogencarbonate; toluene-4-sulfonic acid; tert-butyl alcohol; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/ml200256d
Guidance literature:
Multi-step reaction with 4 steps
1.1: calcium hydride; N-benzyl-N,N,N-triethylammonium chloride / toluene / 48 h / Reflux
2.1: (Dichloroiodo)benzene; tert-butyl alcohol / dichloromethane / 1 h / 0 °C / Photolysis; Inert atmosphere
3.1: pyridine / Reflux
4.1: borane-THF / tetrahydrofuran / 2 h / 0 - 20 °C
4.2: 3 h / 0 °C
4.3: 2 h / 20 °C
With pyridine; calcium hydride; borane-THF; (Dichloroiodo)benzene; N-benzyl-N,N,N-triethylammonium chloride; tert-butyl alcohol; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/ml200256d
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