lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

Base Information

Chemical Name:lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate
CAS No.:1430105-05-7
Molecular Formula:C₁₉H₁₇N₂O₄*Li
Molecular Weight:344.296
Hs Code.:

Synonyms:lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

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Chemical Property of lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

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Technology Process of lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

There total 4 articles about lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate 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:

Reference yield:

: 1430086-19-3
diethyl benzyl({[(1R)-1-phenylethyl]carbamoyl}amino)propanedioate

: 1430105-05-7
lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; methanol; water; for 0.5h;

Reference yield:

: 1430086-18-2
diethyl amino(benzyl)propanedioate trifluoroacetate

: 1430105-05-7
lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16.5 h / 0 - 20 °C

2: lithium hydroxide / tetrahydrofuran; methanol; water / 0.5 h

With N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 100-39-0
benzyl bromide

: 1430105-05-7
lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium ethanolate / ethanol / 6 h

2: dichloromethane / 1 h

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16.5 h / 0 - 20 °C

4: lithium hydroxide / tetrahydrofuran; methanol; water / 0.5 h

With sodium ethanolate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;