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benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<1,4>dioxepine-7-carboxylate

Base Information
  • Chemical Name:benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<1,4>dioxepine-7-carboxylate
  • CAS No.:122881-02-1
  • Molecular Formula:C39H40O8
  • Molecular Weight:636.742
  • Hs Code.:
benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<b,e><1,4>dioxepine-7-carboxylate

Synonyms:

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Chemical Property of benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<1,4>dioxepine-7-carboxylate
Chemical Property:
Purity/Quality:
Safty Information:
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MSDS Files:
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Technology Process of benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<1,4>dioxepine-7-carboxylate

There total 21 articles about benzyl 3-benzyloxy-8-methoxy-6-pentyl-11-oxo-1-(3-oxopentyl)-11H-dibenzo<1,4>dioxepine-7-carboxylate 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 14 steps
1: 95 percent / thionyl chloride, pyridine / CH2Cl2 / 3 h / Ambient temperature
2: 88 percent / dimethylformamide / 7 h / Ambient temperature
3: 91 percent / 30percent aq. sodium hydroxide / methanol / 72 h / Heating
4: 95 percent / potassium carbonate / acetone / 3 h / Heating
5: 95 percent / lithium aluminium hydride / diethyl ether / 2 h / Heating
6: 85 percent / pyridine / CHCl3 / 3 h / 0 °C
7: 94 percent / 1,2-dimethoxyethane / dimethylsulfoxide / 18 h / Ambient temperature
8: 81 percent / ether / benzene / 1 h / Ambient temperature; aq. hydrochloric acid, ethyl acetate, 16 h
9: trifluoroacetic anhydride / nitromethane / 1.5 h / 0 °C
10: H2, conc. hydrichloric acid (4 drops) / 10percent palladized charcoal / ethyl acetate
11: 53 percent / potassium hydrogen carbonate / dimethylformamide / 14 h / Ambient temperature
12: 52 percent / potassium hexacyanoferrate(III), potassium carbonate / H2O; dioxane / 0.17 h
13: 83 percent / various solvent(s) / 0.17 h / Heating
14: 80 percent / potassium carbonate / dimethylformamide / Ambient temperature
With pyridine; hydrogenchloride; sodium hydroxide; lithium aluminium tetrahydride; 1,2-dimethoxyethane; thionyl chloride; diethyl ether; hydrogen; potassium carbonate; potassium hydrogencarbonate; trifluoroacetic anhydride; potassium hexacyanoferrate(III); palladium on activated charcoal; In 1,4-dioxane; methanol; diethyl ether; nitromethane; dichloromethane; chloroform; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; acetone; benzene;
Guidance literature:
Multi-step reaction with 9 steps
1: 83 percent / potassium carbonate / acetone / Heating
2: 100 percent / phosphoryl chloride / 24 h / 70 °C
3: 84 percent / sodium chlorite, sulphamic acid / H2O; dioxane / 0.67 h
4: trifluoroacetic anhydride / nitromethane / 1.5 h / 0 °C
5: H2, conc. hydrichloric acid (4 drops) / 10percent palladized charcoal / ethyl acetate
6: 53 percent / potassium hydrogen carbonate / dimethylformamide / 14 h / Ambient temperature
7: 52 percent / potassium hexacyanoferrate(III), potassium carbonate / H2O; dioxane / 0.17 h
8: 83 percent / various solvent(s) / 0.17 h / Heating
9: 80 percent / potassium carbonate / dimethylformamide / Ambient temperature
With hydrogenchloride; sodium chlorite; aminosulfonic acid; hydrogen; potassium carbonate; potassium hydrogencarbonate; trifluoroacetic anhydride; potassium hexacyanoferrate(III); trichlorophosphate; palladium on activated charcoal; In 1,4-dioxane; nitromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
Guidance literature:
Multi-step reaction with 12 steps
1: 77 percent / potassium carbonate / acetone / 24 h / Heating
2: 89 percent / potassium carbonate / acetone / Heating
3: 80 percent / potassium hydroxide / dimethylsulfoxide; H2O / 16 h / 100 °C
4: 83 percent / potassium carbonate / acetone / Heating
5: 100 percent / phosphoryl chloride / 24 h / 70 °C
6: 84 percent / sodium chlorite, sulphamic acid / H2O; dioxane / 0.67 h
7: trifluoroacetic anhydride / nitromethane / 1.5 h / 0 °C
8: H2, conc. hydrichloric acid (4 drops) / 10percent palladized charcoal / ethyl acetate
9: 53 percent / potassium hydrogen carbonate / dimethylformamide / 14 h / Ambient temperature
10: 52 percent / potassium hexacyanoferrate(III), potassium carbonate / H2O; dioxane / 0.17 h
11: 83 percent / various solvent(s) / 0.17 h / Heating
12: 80 percent / potassium carbonate / dimethylformamide / Ambient temperature
With hydrogenchloride; potassium hydroxide; sodium chlorite; aminosulfonic acid; hydrogen; potassium carbonate; potassium hydrogencarbonate; trifluoroacetic anhydride; potassium hexacyanoferrate(III); trichlorophosphate; palladium on activated charcoal; In 1,4-dioxane; nitromethane; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; acetone;
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