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S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid

Base Information Edit
  • Chemical Name:S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid
  • CAS No.:121410-35-3
  • Molecular Formula:C15H23N3O3
  • Molecular Weight:293.366
  • Hs Code.:
  • Mol file:121410-35-3.mol
S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid

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Chemical Property of S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid Edit
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Technology Process of S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid

There total 4 articles about S-α-phenylethylamide of α-(N-dimethylcarbamoylaminooxy)isobutyric acid 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: 1.) KOH, 2.) SOCl2 / 1.) MeOH, 2.) 20 - 40 deg C, 3.5 h, 3.) CHCl3
2: Et3N / acetonitrile / 1.) 20 deg C, 3 d, 2.) reflux, 7 h
With potassium hydroxide; thionyl chloride; triethylamine; In acetonitrile;
DOI:10.1007/BF00952630
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) KOH, 2.) SOCl2 / 1.) MeOH, 2.) 20 - 40 deg C, 3.5 h, 3.) CHCl3
2: Et3N / acetonitrile / 1.) 20 deg C, 3 d, 2.) reflux, 7 h
With potassium hydroxide; thionyl chloride; triethylamine; In acetonitrile;
DOI:10.1007/BF00952630
Guidance literature:
With triethylamine; In acetonitrile; Yield given. Title compound not separated from byproducts; 1.) 20 deg C, 3 d, 2.) reflux, 7 h;
DOI:10.1007/BF00952630
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