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1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)-

Base Information Edit
  • Chemical Name:1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)-
  • CAS No.:489446-81-3
  • Molecular Formula:C18H24N2O6
  • Molecular Weight:364.39300
  • Hs Code.:
  • Mol file:489446-81-3.mol
1,2-Pyrrolidinedicarboxylic acid,
4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester,
(2R,4S)-

Synonyms:

Suppliers and Price of 1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)-
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 4 raw suppliers
Chemical Property of 1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)- Edit
Chemical Property:
  • PSA:105.17000 
  • LogP:2.70420 
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)-

There total 6 articles about 1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-(phenylmethyl) ester, (2R,4S)- 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 6 steps
1: potassium carbonate / acetone / 4 h / Inert atmosphere; Reflux
2: triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
3: sodium azide / N,N-dimethyl-formamide / 8 h / 60 °C / Inert atmosphere
4: triphenylphosphine; water / tetrahydrofuran
5: sodium hydrogencarbonate / water; 1,4-dioxane / 4 h
6: lithium hydroxide; water / tetrahydrofuran / 1 h
With sodium azide; water; sodium hydrogencarbonate; potassium carbonate; triethylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; acetone; 4: |Staudinger Azide Reduction;
DOI:10.1002/pep2.24140
Guidance literature:
Multi-step reaction with 8 steps
1.1: acetic acid; acetic anhydride / 6 h / Reflux
1.2: 3 h / Reflux
2.1: sodium hydrogencarbonate / water; toluene / 12.5 h / 20 °C
3.1: potassium carbonate / acetone / 4 h / Inert atmosphere; Reflux
4.1: triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
5.1: sodium azide / N,N-dimethyl-formamide / 8 h / 60 °C / Inert atmosphere
6.1: triphenylphosphine; water / tetrahydrofuran
7.1: sodium hydrogencarbonate / water; 1,4-dioxane / 4 h
8.1: lithium hydroxide; water / tetrahydrofuran / 1 h
With sodium azide; water; acetic anhydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene; 6.1: |Staudinger Azide Reduction;
DOI:10.1002/pep2.24140
Guidance literature:
Multi-step reaction with 3 steps
1: triphenylphosphine; water / tetrahydrofuran
2: sodium hydrogencarbonate / water; 1,4-dioxane / 4 h
3: lithium hydroxide; water / tetrahydrofuran / 1 h
With water; sodium hydrogencarbonate; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; water; 1: |Staudinger Azide Reduction;
DOI:10.1002/pep2.24140
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