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Tetraacetylclionamid

Base Information
  • Chemical Name:Tetraacetylclionamid
  • CAS No.:68857-44-3
  • Molecular Formula:C27H26BrN3O8
  • Molecular Weight:600.423
  • Hs Code.:
Tetraacetylclionamid

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Chemical Property of Tetraacetylclionamid
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Technology Process of Tetraacetylclionamid

There total 21 articles about Tetraacetylclionamid 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: 97 percent / NEt3 / dioxane; diethyl ether / 12 h / 0 °C
2: 92 percent / 1N HCl / dioxane; diethyl ether / 0.25 h / 10 °C
3: 83 percent / KI, NaN3 / acetone / 2 h / Ambient temperature
4: 0.5N HCl, H2 / Pd/C (5percent) / ethanol; diethyl ether / 1 h / 2250.2 Torr
5: 86 percent / NEt3 / 0.5 h / 0 °C
6: 90 percent / NaCNBH3 / ethyl acetate; tetrahydrofuran / 12 h / Ambient temperature
7: 86 percent / tri-n-butylphosphan / tetrahydrofuran / 0 °C
8: 79 percent / sodium-metaperiodate / tetrahydrofuran; methanol; H2O / 3 h / Ambient temperature
9: 1) THF, 2) KHCO3 / 1) 1,3-dimethoxybenzene, 0 deg C, 15 min, 2) ethylacetate, 3h, r.t.
With tetrahydrofuran; hydrogenchloride; sodium periodate; sodium azide; tributylphosphine; hydrogen; sodium cyanoborohydride; potassium hydrogencarbonate; triethylamine; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; water; ethyl acetate; acetone;
DOI:10.1002/jlac.198519850414
Guidance literature:
Multi-step reaction with 7 steps
1: 83 percent / KI, NaN3 / acetone / 2 h / Ambient temperature
2: 0.5N HCl, H2 / Pd/C (5percent) / ethanol; diethyl ether / 1 h / 2250.2 Torr
3: 86 percent / NEt3 / 0.5 h / 0 °C
4: 90 percent / NaCNBH3 / ethyl acetate; tetrahydrofuran / 12 h / Ambient temperature
5: 86 percent / tri-n-butylphosphan / tetrahydrofuran / 0 °C
6: 79 percent / sodium-metaperiodate / tetrahydrofuran; methanol; H2O / 3 h / Ambient temperature
7: 1) THF, 2) KHCO3 / 1) 1,3-dimethoxybenzene, 0 deg C, 15 min, 2) ethylacetate, 3h, r.t.
With tetrahydrofuran; hydrogenchloride; sodium periodate; sodium azide; tributylphosphine; hydrogen; sodium cyanoborohydride; potassium hydrogencarbonate; triethylamine; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; water; ethyl acetate; acetone;
DOI:10.1002/jlac.198519850414
Guidance literature:
Multi-step reaction with 8 steps
1: 92 percent / 1N HCl / dioxane; diethyl ether / 0.25 h / 10 °C
2: 83 percent / KI, NaN3 / acetone / 2 h / Ambient temperature
3: 0.5N HCl, H2 / Pd/C (5percent) / ethanol; diethyl ether / 1 h / 2250.2 Torr
4: 86 percent / NEt3 / 0.5 h / 0 °C
5: 90 percent / NaCNBH3 / ethyl acetate; tetrahydrofuran / 12 h / Ambient temperature
6: 86 percent / tri-n-butylphosphan / tetrahydrofuran / 0 °C
7: 79 percent / sodium-metaperiodate / tetrahydrofuran; methanol; H2O / 3 h / Ambient temperature
8: 1) THF, 2) KHCO3 / 1) 1,3-dimethoxybenzene, 0 deg C, 15 min, 2) ethylacetate, 3h, r.t.
With tetrahydrofuran; hydrogenchloride; sodium periodate; sodium azide; tributylphosphine; hydrogen; sodium cyanoborohydride; potassium hydrogencarbonate; triethylamine; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; water; ethyl acetate; acetone;
DOI:10.1002/jlac.198519850414
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