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L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-, bis(phenylmethyl) ester

Base Information Edit
  • Chemical Name:L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-, bis(phenylmethyl) ester
  • CAS No.:63024-02-2
  • Molecular Formula:C33H38N2O8
  • Molecular Weight:590.673
  • Hs Code.:
  • Mol file:63024-02-2.mol
L-Serine,
N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-,
bis(phenylmethyl) ester

Synonyms:

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Chemical Property of L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-, bis(phenylmethyl) ester Edit
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Technology Process of L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-, bis(phenylmethyl) ester

There total 4 articles about L-Serine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-O-(phenylmethyl)-, bis(phenylmethyl) ester 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:
BOC-L-aspartic acid 4-benzyl ester; With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 0 ℃; for 0.5h; under 750.075 Torr; Inert atmosphere;
(S)-benzyl 2-amino-3-(benzyloxy)propanoate hydrochloride; With 4-methyl-morpholine; In tetrahydrofuran; at 0 - 20 ℃; under 750.075 Torr; pH=8.5; Inert atmosphere;
DOI:10.1016/j.ejmech.2008.09.036
Guidance literature:
Multi-step reaction with 3 steps
1.1: caesium carbonate / water; ethanol / 0.25 h / 20 °C
1.2: 4 h / 55 - 60 °C
2.1: hydrogenchloride / ethyl acetate / 2 h / 0 °C
3.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / tetrahydrofuran / 0.33 h / 0 °C
3.2: 24 h / 20 °C
With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethanol; water; ethyl acetate;
DOI:10.1039/c5md00215j
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogenchloride / ethyl acetate / 2 h / 0 °C
2.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / tetrahydrofuran / 0.33 h / 0 °C
2.2: 24 h / 20 °C
With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethyl acetate;
DOI:10.1039/c5md00215j
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