(4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone

Base Information

• Chemical Name: (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone
• CAS No.: 861640-62-2
• Molecular Formula: C₂₇H₃₁NO₄Si
• Molecular Weight: 461.633

Synonyms:(4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone

Chemical Property of (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone

Chemical Property:

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Technology Process of (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone

There total 5 articles about (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-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: 98.0%

(4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propen-1-yl]-4-phenyl-2-oxazolidinone (861640-61-1) → (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone (861640-62-2)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethyl acetate; at 20 ℃; for 24h;

DOI:10.1016/j.bmc.2005.04.028

Reference yield:

(4S)-3-[3-(5-hydroxy-1-naphthalenyl)-1-oxo-2-propen-1-yl]-4-phenyl-2-oxazolidinone (861640-60-0) → (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone (861640-62-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 49 percent / triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 24 h / 20 °C

2: 98 percent / H₂ / Pd/C / ethyl acetate / 24 h / 20 °C

With hydrogen; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/j.bmc.2005.04.028

Reference yield:

2-(Trimethylsilyl)ethanol (2916-68-9) → (4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propan-1-yl]-4-phenyl-2-oxazolidinone (861640-62-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 49 percent / triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 24 h / 20 °C

2: 98 percent / H₂ / Pd/C / ethyl acetate / 24 h / 20 °C

With hydrogen; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/j.bmc.2005.04.028

upstream raw materials:

(4S)-3-[3-(5-(2-(trimethylsilyl)ethyl)oxy-1-naphthalenyl)-1-oxo-2-propen-1-yl]-4-phenyl-2-oxazolidinone

(4S)-3-[3-(5-hydroxy-1-naphthalenyl)-1-oxo-2-propen-1-yl]-4-phenyl-2-oxazolidinone

2-(Trimethylsilyl)ethanol

5-bromo-1-naphthol

Downstream raw materials:

C₆₇H₉₆N₇O₁₃PS

(βS,γS)-β-[[1-[[(1S)-3-amino-1-[[(2S)-2-(5-hydroxy-1-naphthalenylmethyl)-4-pentenyl]aminocarbonyl]-3-oxopropyl]aminocarbonyl]cyclohexyl]aminocarbonyl]-4-[4-[bis(tert-butoxy)phosphoryl]methyl]-γ-ethenylbenzenebutanoic acid 1,1-dimethylethyl ester

(9S,10S,11E,14S,18S)-18-(2-amino-2-oxoethyl)-10-[[4-[bis(1,1-dimethylethoxy)phosphoryl]methyl]phenyl]-14-(1-(5-hydroxy)naphthalenylmethyl)-8,17,20-trioxo-7,16,19-triazaspiro[5.14]eicos-11-en-9-acetic acid 1,1-dimethylethyl ester

(2S)-2-[[(1-aminocyclohexyl)carbonyl]amino]-N¹-[(2S)-2-(5-hydroxy-1-naphthalenylmethyl)-4-pentenyl]butanediamide

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