[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

Base Information

Chemical Name:[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone
CAS No.:287400-78-6
Molecular Formula:C₂₉H₄₇NO₆Si
Molecular Weight:533.781
Hs Code.:

Synonyms:[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

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Chemical Property of [3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

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Technology Process of [3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

There total 3 articles about [3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone 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: 95.0%

: 994-30-9
triethylsilyl chloride

: 287400-77-5
[3(2S,3R),4S]-3-(3-hydroxy-2-methyl-1-oxo-6-trimethyl-acetoxyheptanyl)-4-(phenylmethyl)-2-oxazolidinone

: 287400-78-6
[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 0.333333h;
DOI:10.1021/jo0002801

Reference yield:

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

: 287400-78-6
[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / Bu₂BOTf; diisopropylethylamine / CH₂Cl₂ / -78 - 0 °C

2: 95 percent / imidazole / dimethylformamide / 0.33 h / 0 °C

With 1H-imidazole; di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; 1: Condensation / 2: silylation;
DOI:10.1021/jo0002801

Reference yield:

: 287401-05-2
5-oxopentyl-2',2'-dimethylpropanoate

: 287400-78-6
[3(2S,3R),4S]-3-[2-methyl-1-oxo-3-[(triethylsilyl)oxy]-6-trimethylacetoxy-heptanyl]-4-(phenylmethyl)-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / Bu₂BOTf; diisopropylethylamine / CH₂Cl₂ / -78 - 0 °C

2: 95 percent / imidazole / dimethylformamide / 0.33 h / 0 °C

With 1H-imidazole; di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; 1: Condensation / 2: silylation;
DOI:10.1021/jo0002801