(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

Base Information

Chemical Name:(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one
CAS No.:947696-78-8
Molecular Formula:C₄₄H₆₅NO₆Si₂
Molecular Weight:760.174
Hs Code.:

Synonyms:(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

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Chemical Property of (4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

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Technology Process of (4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

There total 7 articles about (4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-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:

: 947696-75-5
(4R,5S)-4-methyl-5-phenyl-3-[(2R,3S,6S)-7-(tert-butyldiphenylsilyloxy)-3-hydroxy-2,6-dimethylheptanoyl]-1,3-oxazolidin-2-one

: 947696-78-8
(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: Me₃Al / tetrahydrofuran; toluene / 1 h / 20 °C

1.2: 79 percent / tetrahydrofuran; toluene / 3 h / 20 °C

2.1: 92 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 20 °C

3.1: diisobutylaluminum hydride / tetrahydrofuran; hexane / 0.5 h / -78 °C

4.1: 3.53 g / CH₂Cl₂ / 3 h / 0 °C

With 2,6-dimethylpyridine; trimethylaluminum; diisobutylaluminium hydride; In tetrahydrofuran; hexane; dichloromethane; toluene; 4.1: Evans asymmetric aldolization;
DOI:10.1002/chem.200700342

Reference yield:

: 131685-53-5,101711-78-8
(S)-4-benzyl-3-propionyl-2-oxazolidinone

: 947696-78-8
(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1.5 h / -78 - 0 °C

2: 3.53 g / CH₂Cl₂ / 3 h / 0 °C

With triethylamine; In dichloromethane; 2: Evans asymmetric aldolization;
DOI:10.1002/chem.200700342

Reference yield:

: 123444-68-8
(S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutanal

: 947696-78-8
(4S)-4-benzyl-3-[(2S,3R,4S,5S,8S)-5-(tert-butyldimethylsilyloxy)-9-(tert-butyldiphenylsilyloxy)-2,4,8-trimethylnonanoyl]-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: 5.23 g / CH₂Cl₂ / 2.5 h / 0 °C

2.1: Me₃Al / tetrahydrofuran; toluene / 1 h / 20 °C

2.2: 79 percent / tetrahydrofuran; toluene / 3 h / 20 °C

3.1: 92 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 20 °C

4.1: diisobutylaluminum hydride / tetrahydrofuran; hexane / 0.5 h / -78 °C

5.1: 3.53 g / CH₂Cl₂ / 3 h / 0 °C

With 2,6-dimethylpyridine; trimethylaluminum; diisobutylaluminium hydride; In tetrahydrofuran; hexane; dichloromethane; toluene; 1.1: Evans asymmetric aldolization / 5.1: Evans asymmetric aldolization;
DOI:10.1002/chem.200700342