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benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate

Base Information Edit
  • Chemical Name:benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate
  • CAS No.:116129-89-6
  • Molecular Formula:C22H25NO4
  • Molecular Weight:367.445
  • Hs Code.:
  • Mol file:116129-89-6.mol
benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate

Synonyms:benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate

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Chemical Property of benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate Edit
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Technology Process of benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate

There total 6 articles about benzyl (2R)-2-Benzyl-3-morpholinocarbonylpropionate 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 4-methyl-morpholine; isobutyl chloroformate; Multistep reaction; 1.) CH2Cl2, 0-20 deg C, 30 min, 2.) CH2Cl2, RT, overnight;
DOI:10.1021/jm00088a005
Guidance literature:
Multi-step reaction with 2 steps
1: 100 percent / trifluoroacetic acid / CH2Cl2 / 1 h / Ambient temperature
2: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) THF, 5 min, 2.) 1 h
With 4-methyl-morpholine; trifluoroacetic acid; isobutyl chloroformate; In dichloromethane;
DOI:10.1021/jm00120a006
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) sodium hexamethyldisilylamide / 1.) THF, -78 deg C, 30 min, 2.) -78 deg C, 1 h
2: 94 percent / n-butyllithium / tetrahydrofuran / 1 h / 0 °C
3: 100 percent / trifluoroacetic acid / CH2Cl2 / 1 h / Ambient temperature
4: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) THF, 5 min, 2.) 1 h
With 4-methyl-morpholine; n-butyllithium; sodium hexamethyldisilazane; trifluoroacetic acid; isobutyl chloroformate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00120a006
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