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

Encyclopedia

methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate

Base Information Edit
  • Chemical Name:methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate
  • CAS No.:1383786-67-1
  • Molecular Formula:C20H21NO7
  • Molecular Weight:387.389
  • Hs Code.:
  • Mol file:1383786-67-1.mol
methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate

Synonyms:methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate

Suppliers and Price of methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate
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 methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate

There total 7 articles about methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate 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:
5-methoxy-2-methoxycarbonylmethyl-benzoic acid methyl ester; With n-butyllithium; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at -78 - 0 ℃; for 1.16667h; Inert atmosphere;
With carbon dioxide; In tetrahydrofuran; for 1h;
N-benzyloxyamine;
Guidance literature:
Multi-step reaction with 5 steps
1.1: nitric acid / 2 h / 0 - 22 °C
2.1: methanol; hydrogen / 5%-palladium/activated carbon / 0.08 h / 760.05 Torr / Reflux
3.1: sulfuric acid; sodium nitrite / water / 2 h / 0 - 5 °C / Cooling with ice
4.1: thionyl chloride / 24 h / Reflux
4.2: 12 h / Reflux
5.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.17 h / -78 - 0 °C / Inert atmosphere
5.2: 1 h
With methanol; n-butyllithium; thionyl chloride; sulfuric acid; hydrogen; nitric acid; N-ethyl-N,N-diisopropylamine; sodium nitrite; 5%-palladium/activated carbon; In tetrahydrofuran; water;
Guidance literature:
Multi-step reaction with 4 steps
1.1: methanol; hydrogen / 5%-palladium/activated carbon / 0.08 h / 760.05 Torr / Reflux
2.1: sulfuric acid; sodium nitrite / water / 2 h / 0 - 5 °C / Cooling with ice
3.1: thionyl chloride / 24 h / Reflux
3.2: 12 h / Reflux
4.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.17 h / -78 - 0 °C / Inert atmosphere
4.2: 1 h
With methanol; n-butyllithium; thionyl chloride; sulfuric acid; hydrogen; N-ethyl-N,N-diisopropylamine; sodium nitrite; 5%-palladium/activated carbon; In tetrahydrofuran; water;
Post RFQ for Price