(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

Base Information

Chemical Name:(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one
CAS No.:159164-13-3
Molecular Formula:C₃₂H₃₉NO₅Si
Molecular Weight:545.751
Hs Code.:

Synonyms:(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

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Chemical Property of (4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

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Technology Process of (4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

There total 5 articles about (4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-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%

: 17690-16-3
benzyl bromomethyl ether

: 159164-12-2
(4R,5S)-3-{2-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-acetyl}-4-methyl-5-phenyl-oxazolidin-2-one

: 159164-13-3
(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/S0957-4166(00)86199-6

Reference yield:

: 79302-24-2
4-[(trimethylsilyl)oxy]benzeneacetyl chloride

: 159164-13-3
(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / -78 °C

2: 10percent aq. HCl

3: imidazole

4: 67 percent / 1.) LDA / tetrahydrofuran / -78 °C

With 1H-imidazole; hydrogenchloride; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1016/S0957-4166(00)86199-6

Reference yield:

: 27750-57-8
4-[(trimethylsilyl)oxy]benzeneacetic acid (trimethylsilyl) ester

: 159164-13-3
(4R,5S)-3-{(S)-3-Benzyloxy-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: SOCl₂

2: tetrahydrofuran / -78 °C

3: 10percent aq. HCl

4: imidazole

5: 67 percent / 1.) LDA / tetrahydrofuran / -78 °C

With 1H-imidazole; hydrogenchloride; thionyl chloride; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1016/S0957-4166(00)86199-6