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

Encyclopedia

1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate

Base Information Edit
  • Chemical Name:1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate
  • CAS No.:1357010-68-4
  • Molecular Formula:C26H39NO7
  • Molecular Weight:477.598
  • Hs Code.:
  • Mol file:1357010-68-4.mol
1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate

Synonyms:1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate

Suppliers and Price of 1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate
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 1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate

There total 5 articles about 1-tert-butyl 4-ethyl 2-(2-benzyloxycarbonylamino-3-ethylpentanoyl)-3-methylsuccinate 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:
tert-butyl 4-benzyloxycarbonylamino-5-ethyl-3-oxoheptanoate; With sodium hydride; In tetrahydrofuran; mineral oil; at 0 ℃; for 0.166667h;
rac-2-(Trifluormethylsulfonyloxy)propionsaeure-ethylester; In tetrahydrofuran; dichloromethane; mineral oil; at 20 ℃; for 2h;
DOI:10.1016/j.bmc.2011.11.015
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydrogensulfite / methanol; water / 12 h / 60 °C
2.1: hydrogen bromide / 2 h / 150 °C
3.1: sodium hydroxide / 17 h / 20 °C
4.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C
4.2: 1.5 h / -78 - 20 °C
5.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 0 °C
5.2: 2 h / 20 °C
With hydrogen bromide; sodium hydride; sodium hydrogensulfite; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; water; mineral oil;
DOI:10.1016/j.bmc.2011.11.015
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydroxide / 17 h / 20 °C
2.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C
2.2: 1.5 h / -78 - 20 °C
3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 0 °C
3.2: 2 h / 20 °C
With sodium hydride; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; mineral oil;
DOI:10.1016/j.bmc.2011.11.015
Refernces Edit
Post RFQ for Price