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1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl ether

Base Information
  • Chemical Name:1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl ether
  • CAS No.:88908-60-5
  • Molecular Formula:C39H42O4
  • Molecular Weight:574.76
  • Hs Code.:
1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl ether

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Chemical Property of 1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl ether
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Technology Process of 1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl ether

There total 11 articles about 1,3,5(10)-estratriene-2,3,7α,17β-tetraol 2,3,17-tribenzyl 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 9 steps
1: 1.) pyridinium chloride / 1.) 1 h, 200 deg C; 2.) pyridine, 1 h, r.t.
2: 56 percent / CrO3 / acetic acid; H2O / 1 h / 0 °C
3: 54 percent / NaBH4 / tetrahydrofuran; ethanol / 1.5 h
4: 93 percent / K2CO3 / dimethylformamide / 16 h
5: 89 percent / KOH / methanol / 2 h
6: 57 percent / 50percent NaH / dimethylformamide
7: CH2Cl2 / 0.17 h / 0 °C
8: 1 N NaOH / tetrahydrofuran; methanol / 1 h
9: 1.) thionyl chloride; 2.) LiAlH4 / 1.) THF, 0 deg C, 1 h; 2.) THF, reflux, 1 h
With chromium(VI) oxide; potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; thionyl chloride; pyridine hydrochloride; sodium hydride; potassium carbonate; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide;
DOI:10.1002/recl.19831021003
Guidance literature:
Multi-step reaction with 8 steps
1: 56 percent / CrO3 / acetic acid; H2O / 1 h / 0 °C
2: 54 percent / NaBH4 / tetrahydrofuran; ethanol / 1.5 h
3: 93 percent / K2CO3 / dimethylformamide / 16 h
4: 89 percent / KOH / methanol / 2 h
5: 57 percent / 50percent NaH / dimethylformamide
6: CH2Cl2 / 0.17 h / 0 °C
7: 1 N NaOH / tetrahydrofuran; methanol / 1 h
8: 1.) thionyl chloride; 2.) LiAlH4 / 1.) THF, 0 deg C, 1 h; 2.) THF, reflux, 1 h
With chromium(VI) oxide; potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; thionyl chloride; sodium hydride; potassium carbonate; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide;
DOI:10.1002/recl.19831021003
Guidance literature:
Multi-step reaction with 4 steps
1: 57 percent / 50percent NaH / dimethylformamide
2: CH2Cl2 / 0.17 h / 0 °C
3: 1 N NaOH / tetrahydrofuran; methanol / 1 h
4: 1.) thionyl chloride; 2.) LiAlH4 / 1.) THF, 0 deg C, 1 h; 2.) THF, reflux, 1 h
With sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; sodium hydride; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/recl.19831021003
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