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N-tert-butyloxycarbonyl-O-benzyl serine nitrile

Base Information Edit
  • Chemical Name:N-tert-butyloxycarbonyl-O-benzyl serine nitrile
  • CAS No.:244778-26-5
  • Molecular Formula:C15H20N2O3
  • Molecular Weight:276.335
  • Hs Code.:
  • Mol file:244778-26-5.mol
N-tert-butyloxycarbonyl-O-benzyl serine nitrile

Synonyms:N-tert-butyloxycarbonyl-O-benzyl serine nitrile

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Chemical Property of N-tert-butyloxycarbonyl-O-benzyl serine nitrile Edit
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Technology Process of N-tert-butyloxycarbonyl-O-benzyl serine nitrile

There total 7 articles about N-tert-butyloxycarbonyl-O-benzyl serine nitrile 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 trifluoroacetic anhydride; In pyridine; at 0 ℃; for 2.5h;
Guidance literature:
Multi-step reaction with 4 steps
1.1: NaH / dimethylformamide / 0.58 h / 0 - 20 °C
1.2: dimethylformamide / 0.5 h / 0 - 20 °C
2.1: N-methylmorpholine / CH2Cl2 / 0.25 h
3.1: NH3(g) / CH2Cl2 / 0.25 h
4.1: oxalyl chloride; pyridine / dimethylformamide / 0.75 h / 0 °C
With 4-methyl-morpholine; pyridine; oxalyl dichloride; ammonia; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm010206q
Guidance literature:
Multi-step reaction with 3 steps
1: N-methylmorpholine / CH2Cl2 / 0.25 h
2: NH3(g) / CH2Cl2 / 0.25 h
3: oxalyl chloride; pyridine / dimethylformamide / 0.75 h / 0 °C
With 4-methyl-morpholine; pyridine; oxalyl dichloride; ammonia; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm010206q
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