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

Encyclopedia

5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid

Base Information Edit
  • Chemical Name:5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid
  • CAS No.:1259391-12-2
  • Molecular Formula:C30H31NO6
  • Molecular Weight:501.579
  • Hs Code.:
  • Mol file:1259391-12-2.mol
5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid

Synonyms:5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid

Suppliers and Price of 5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid
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 5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid

There total 6 articles about 5-((S)-2-benzyl-3-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl)-2-propoxybenzoic acid 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 palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 3h; under 735.074 Torr;
DOI:10.1021/jm101233f
Guidance literature:
Multi-step reaction with 2 steps
1.1: sodium hexamethyldisilazane / tetrahydrofuran / -50 - -15 °C / Inert atmosphere
1.2: -50 - 20 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 3 h / 20 °C / 735.07 Torr
With palladium 10% on activated carbon; hydrogen; sodium hexamethyldisilazane; In tetrahydrofuran; ethyl acetate; 1.1: Evan's asymmetric alkylation / 1.2: Evan's asymmetric alkylation;
DOI:10.1021/jm101233f
Guidance literature:
Multi-step reaction with 6 steps
1.1: potassium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 20 °C
2.1: potassium carbonate / N,N-dimethyl-formamide / 24 h / 60 °C
3.1: sodium tetrahydroborate / ethanol / 0 - 20 °C
4.1: phosphorus tribromide / diethyl ether / 1.5 h / 0 °C
5.1: sodium hexamethyldisilazane / tetrahydrofuran / -50 - -15 °C / Inert atmosphere
5.2: -50 - 20 °C / Inert atmosphere
6.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 3 h / 20 °C / 735.07 Torr
With sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; sodium hexamethyldisilazane; phosphorus tribromide; potassium carbonate; potassium hydrogencarbonate; In tetrahydrofuran; diethyl ether; ethanol; ethyl acetate; N,N-dimethyl-formamide; 5.1: Evan's asymmetric alkylation / 5.2: Evan's asymmetric alkylation;
DOI:10.1021/jm101233f
Post RFQ for Price