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methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate

Base Information
  • Chemical Name:methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate
  • CAS No.:350689-56-4
  • Molecular Formula:C37H48F17NO4
  • Molecular Weight:893.765
  • Hs Code.:
methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate

Synonyms:methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate

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Chemical Property of methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate
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Technology Process of methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate

There total 5 articles about methyl N-[2-(benzyloxy)ethyl]-N-[7-(F-octyl)heptyl]-11-carboxamidoundecanoate 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 triethylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jm0011124
Guidance literature:
Multi-step reaction with 2 steps
1: Ba(OH)2
2: 78 percent / PyBrop; Et3N / CH2Cl2 / 0 - 20 °C
With barium dihydroxide; triethylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In dichloromethane;
DOI:10.1021/jm0011124
Guidance literature:
Multi-step reaction with 3 steps
1: 95 percent / Et3N; HOBt; EDC / CH2Cl2 / 0 - 20 °C
2: 80 percent / LiAlH4 / tetrahydrofuran / 24 h / 20 °C
3: 78 percent / PyBrop; Et3N / CH2Cl2 / 0 - 20 °C
With lithium aluminium tetrahydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm0011124
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