Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate

Base Information Edit
  • Chemical Name:tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate
  • CAS No.:1381964-05-1
  • Molecular Formula:C25H25BrClNO3
  • Molecular Weight:502.835
  • Hs Code.:
  • Mol file:1381964-05-1.mol
tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate

Synonyms:tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate

Suppliers and Price of tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 0 raw suppliers
Chemical Property of tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-carboxylate

There total 5 articles about tert-butyl 1,2-dihydro-5-(benzyloxy)-6-bromo-1-(chloromethyl)-1H-benzo[e]indole-3(2H)-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:
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; at 80 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jm300330b
Guidance literature:
Multi-step reaction with 5 steps
1.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 24 h / 25 °C
2.1: diphenyl phosphoryl azide; triethylamine / 14 h / 85 °C / Inert atmosphere
3.1: N-iodo-succinimide; toluene-4-sulfonic acid / tetrahydrofuran / 2 h / 25 °C / Inert atmosphere; Darkness
4.1: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C
4.2: 1 h / 20 °C
5.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / 12 h / 80 °C / Inert atmosphere
With N-iodo-succinimide; lithium hydroxide monohydrate; 2,2'-azobis(isobutyronitrile); diphenyl phosphoryl azide; water; tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; mineral oil; benzene;
DOI:10.1021/jm300330b
Guidance literature:
Multi-step reaction with 7 steps
1.1: potassium carbonate / ethanol / 1 h / 80 °C
2.1: tetra-(n-butyl)ammonium iodide; potassium carbonate / N,N-dimethyl-formamide / 16 h / 25 °C
3.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 24 h / 25 °C
4.1: diphenyl phosphoryl azide; triethylamine / 14 h / 85 °C / Inert atmosphere
5.1: N-iodo-succinimide; toluene-4-sulfonic acid / tetrahydrofuran / 2 h / 25 °C / Inert atmosphere; Darkness
6.1: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C
6.2: 1 h / 20 °C
7.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / 12 h / 80 °C / Inert atmosphere
With N-iodo-succinimide; lithium hydroxide monohydrate; 2,2'-azobis(isobutyronitrile); diphenyl phosphoryl azide; water; tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; mineral oil; benzene;
DOI:10.1021/jm300330b
Post RFQ for Price