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dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide

Base Information
  • Chemical Name:dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide
  • CAS No.:934807-99-5
  • Molecular Formula:C32H53N3O
  • Molecular Weight:495.792
  • Hs Code.:
dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide

Synonyms:dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide

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Chemical Property of dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide
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Technology Process of dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide

There total 5 articles about dec-9-enoic acid (3-{[4-(2-allyl-piperidin-1-yl)-butyl]-benzyl-amino}-propyl)-amide 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 3 steps
1: 87 percent / triethylamine; DMAP; benzoic anhydride / CH2Cl2 / 25 h / 20 °C
2: lithium aluminum hydride / 25 °C
3: 276 mg / triethylamine / CH2Cl2 / 2 h / 0 °C
With dmap; lithium aluminium tetrahydride; benzoic acid anhydride; triethylamine; In dichloromethane; 2: retro-Michael addition;
DOI:10.1016/j.tet.2007.01.068
Guidance literature:
Multi-step reaction with 2 steps
1: lithium aluminum hydride / 25 °C
2: 276 mg / triethylamine / CH2Cl2 / 2 h / 0 °C
With lithium aluminium tetrahydride; triethylamine; In dichloromethane; 1: retro-Michael addition;
DOI:10.1016/j.tet.2007.01.068
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