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Acetamide, N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)-

Base Information
  • Chemical Name:Acetamide, N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)-
  • CAS No.:562870-89-7
  • Molecular Formula:C16H20F3NO2
  • Molecular Weight:315.336
  • Hs Code.:
Acetamide,
N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)-

Synonyms:

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Chemical Property of Acetamide, N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)-
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Technology Process of Acetamide, N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)-

There total 8 articles about Acetamide, N-[(1S)-1-ethenyl-3-methylbutyl]-2,2,2-trifluoro-N-(4-methoxyphenyl)- 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 C108H88Cl4Fe2N8O8Pd2Pt2S4; C108H88Cl4Fe2N8O8Pd2Pt2S4; silver(I) 4-methylbenzenesulfonate; In chloroform; at 55 ℃; for 72h; Concentration; Reagent/catalyst; Temperature; enantioselective reaction; Catalytic behavior; Inert atmosphere; Sealed tube;
DOI:10.1021/om300600v
Guidance literature:
With silver(I) 4-methylbenzenesulfonate; chiral ferrocenyl-bisimidazoline palladacycle; In chloroform; at 55 ℃; for 72h;
DOI:10.1002/anie.200603568
Guidance literature:
With chiral palladim(II)-based; In dichloromethane; at 23 ℃; for 60h; Title compound not separated from byproducts;
DOI:10.1021/ol0271786
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