(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

Base Information

Chemical Name:(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one
CAS No.:163127-73-9
Molecular Formula:C₂₁H₂₄N₄O₃Si
Molecular Weight:408.532
Hs Code.:

Synonyms:(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

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Chemical Property of (4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

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Technology Process of (4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

There total 10 articles about (4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one 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: 67.0%

: 163127-85-3
(4R,2'S)-4-benzyl-3-{2-bromo-3-[(dimethyl)phenylsilyl]propionyl}oxazolidin-2-one

: 163127-73-9
(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

Guidance literature:: With N,N,N',N'-tetramethylguanidinium azide; In acetonitrile; at 0 ℃; for 4h;
DOI:10.1016/S0957-4166(01)00028-3

Reference yield:

: (4R,2'S)-4-Benzyl-3-<2'-bromo-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

: 163127-73-9
(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

Guidance literature:: With tetramethylguanidinum azide; In acetonitrile; at 0 ℃; for 2h; Yield given;
DOI:10.1021/jo00113a053

Reference yield:

: 59344-04-6
methyl 3-[(dimethyl)phenylsilyl]propionate

: 163127-73-9
(4R,2'S)-4-Benzyl-3-<2'-azido-3'-(dimethylphenylsilyl)propanoyl>-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / aq. LiOH / tetrahydrofuran / 15 h / 23 °C

2: NaH / tetrahydrofuran / 2 h / 0 °C

3: 1.04 g / BuLi / hexane; tetrahydrofuran / 3.5 h / -78 - 23 °C

4: DIPEA / CH₂Cl₂ / 4 h / -78 - 0 °C

5: 0.91 g / NBS / CH₂Cl₂ / 2 h / -78 °C

6: 67 percent / N,N,N',N'-tetramethylguanidinium azide / acetonitrile / 4 h / 0 °C

With lithium hydroxide; N-Bromosuccinimide; n-butyllithium; N,N,N',N'-tetramethylguanidinium azide; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1016/S0957-4166(01)00028-3