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methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate

Base Information Edit
  • Chemical Name:methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate
  • CAS No.:95230-30-1
  • Molecular Formula:C38H46O12
  • Molecular Weight:694.776
  • Hs Code.:
  • Mol file:95230-30-1.mol
methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate

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Chemical Property of methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate Edit
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Technology Process of methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate

There total 7 articles about methyl (3-benzyloxy-17β-hydroxyestra-1,3,5(10)trien-11α-yl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate 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
1: 980 mg / 2,3-dichloro-5,6-dicyanobenzoquinone / methanol / 0.17 h / Ambient temperature
2: 860 mg / toluene-p-sulphonic acid / benzene / 2 h / Heating
3: 1.) diborane, 2.) 30percent aq. hydrogen peroxide, aq. sodium hydroxide / 1.) tetrahydrofuran, room temperature, 2 h, 2.) room temperature, overnight
4: 280 mg / toluene-p-sulphonic acid / methanol / 0.33 h / Heating
5: 220 mg / sodium hydroxide / ethanol / 1.5 h / Heating
6: 35 percent / cadmium carbonate / benzene / 2 h / Heating
7: 260 mg / sodium borohydride / methanol / 0.08 h / 5 °C
With sodium hydroxide; sodium tetrahydroborate; cadmium(II) carbonate; dihydrogen peroxide; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; diborane; In methanol; ethanol; benzene;
DOI:10.1039/P19840002595
Guidance literature:
Multi-step reaction with 6 steps
1: 860 mg / toluene-p-sulphonic acid / benzene / 2 h / Heating
2: 1.) diborane, 2.) 30percent aq. hydrogen peroxide, aq. sodium hydroxide / 1.) tetrahydrofuran, room temperature, 2 h, 2.) room temperature, overnight
3: 280 mg / toluene-p-sulphonic acid / methanol / 0.33 h / Heating
4: 220 mg / sodium hydroxide / ethanol / 1.5 h / Heating
5: 35 percent / cadmium carbonate / benzene / 2 h / Heating
6: 260 mg / sodium borohydride / methanol / 0.08 h / 5 °C
With sodium hydroxide; sodium tetrahydroborate; cadmium(II) carbonate; dihydrogen peroxide; toluene-4-sulfonic acid; diborane; In methanol; ethanol; benzene;
DOI:10.1039/P19840002595
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