(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

Base Information

Chemical Name:(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester
CAS No.:219992-26-4
Molecular Formula:C₂₁H₂₅NO₅
Molecular Weight:371.433
Hs Code.:

Synonyms:(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

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Chemical Property of (2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

Chemical Property:

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Technology Process of (2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

There total 4 articles about (2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl 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:

Reference yield:

: 65564-05-8
3-[(benzyloxycarbonyl)amino]propanal

: 219992-26-4
(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) di-n-butylboryltriflate, 2.) DPEA

2: aq. 30percent H₂O₂, aq. LiOH / tetrahydrofuran / 1 h / 0 °C

3: HCl / Ambient temperature

With hydrogenchloride; lithium hydroxide; di-n-butylboryl trifluoromethanesulfonate; dihydrogen peroxide; In tetrahydrofuran;
DOI:10.1021/ja983063e

Reference yield:

: 95841-14-8
(4R,5S)-3-(3-phenylpropionyl)-4-methyl-5-phenyl-oxazolidin-2-one

: 219992-26-4
(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) di-n-butylboryltriflate, 2.) DPEA

2: aq. 30percent H₂O₂, aq. LiOH / tetrahydrofuran / 1 h / 0 °C

3: HCl / Ambient temperature

With hydrogenchloride; lithium hydroxide; di-n-butylboryl trifluoromethanesulfonate; dihydrogen peroxide; In tetrahydrofuran;
DOI:10.1021/ja983063e

Reference yield:

: 219992-25-3
[(3S,4R)-4-Benzyl-3-hydroxy-5-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-5-oxo-pentyl]-carbamic acid benzyl ester

: 219992-26-4
(2R,3S)-2-Benzyl-5-benzyloxycarbonylamino-3-hydroxy-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. 30percent H₂O₂, aq. LiOH / tetrahydrofuran / 1 h / 0 °C

2: HCl / Ambient temperature

With hydrogenchloride; lithium hydroxide; dihydrogen peroxide; In tetrahydrofuran;
DOI:10.1021/ja983063e