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N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide

Base Information Edit
  • Chemical Name:N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide
  • CAS No.:1449608-01-8
  • Molecular Formula:C24H22BrNO
  • Molecular Weight:420.349
  • Hs Code.:
  • Mol file:1449608-01-8.mol
N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide Edit
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Technology Process of N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide

There total 2 articles about N-benzyl-N-(1-(1-bromonaphthalen-2-yl)allyl)methacrylamide 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 2 steps
1: copper(l) chloride / acetonitrile / 0.5 h / 20 °C / Inert atmosphere
2: dichloromethane / 6 h / 45 °C / Inert atmosphere
With copper(l) chloride; In dichloromethane; acetonitrile;
DOI:10.1021/jo400974k
Guidance literature:
In dichloromethane; at 45 ℃; for 6h; Inert atmosphere;
DOI:10.1021/jo400974k
Guidance literature:
With tetrabutyl-ammonium chloride; palladium diacetate; sodium carbonate; In N,N-dimethyl-formamide; at 80 ℃; Overall yield = 65 %; Overall yield = 123 mg; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/jo400974k
upstream raw materials:

tri-n-butyl(vinyl)tin

C18H14BrN

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