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

Encyclopedia

(3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione

Base Information Edit
  • Chemical Name:(3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione
  • CAS No.:944543-96-8
  • Molecular Formula:C26H25NO5
  • Molecular Weight:431.488
  • Hs Code.:
  • Mol file:944543-96-8.mol
(3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione

Synonyms:(3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione

Suppliers and Price of (3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione
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 (3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione

There total 1 articles about (3S,4S)-1-(4-methoxybenzyl)-3,4-dibenzyloxy-2,5-pyrrolidinedione 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:
L-O,O-dibenzyltartaric acid; With acetyl chloride; for 4h; Heating;
4-methoxy-benzylamine; In dichloromethane; for 5h; Heating;
With acetyl chloride; for 6h; Further stages.; Heating;
DOI:10.1016/j.tet.2007.02.087
Guidance literature:
With magnesium; mercury dichloride; In tetrahydrofuran; at 20 ℃; for 7h;
DOI:10.1016/j.tet.2007.02.087
Guidance literature:
Multi-step reaction with 5 steps
1: 81 percent / magnesium; mercury(II) chloride / tetrahydrofuran / 7 h / 20 °C
2: 777 mg / triethylsilane; boron trifluoride etherate / CH2Cl2 / -78 - 20 °C
3: 85 percent / ceric ammonium nitrate / acetonitrile; H2O / 5.5 h / 0 - 20 °C
4: 10 percent / BH3*SMe2 / tetrahydrofuran / 0 - 20 °C
5: 80 percent / K2CO3 / methanol / 48 h / 20 °C
With triethylsilane; ammonium cerium(IV) nitrate; dimethylsulfide borane complex; boron trifluoride diethyl etherate; potassium carbonate; magnesium; mercury dichloride; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile; 1: Grignard reaction;
DOI:10.1016/j.tet.2007.02.087
Post RFQ for Price