(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

Base Information

Chemical Name:(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one
CAS No.:444200-04-8
Molecular Formula:C₂₇H₄₅NO₆Si
Molecular Weight:507.743
Hs Code.:

Synonyms:(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

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Chemical Property of (4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

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Technology Process of (4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

There total 2 articles about (4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-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: 87.0%

: 107-30-2
chloromethyl methyl ether

: 444200-03-7
(4S)-4-benzyl-3-{(2S,3R)-3-hydroxy-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

: 444200-04-8
(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

Guidance literature:: With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/ol026040k

Reference yield:

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

: 444200-04-8
(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: titanium(IV) chloride; (-)-sparteine / CH₂Cl₂ / 0.33 h / 0 °C

1.2: 88 percent / 1 h / 0 °C

2.1: 87 percent / N,N-diisopropylethyamine; tetrabutylammonium iodide / CH₂Cl₂ / 18 h / 20 °C

With titanium tetrachloride; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; (-)-sparteine; In dichloromethane; 1.2: Evans aldol reaction;
DOI:10.1021/ol026040k

Reference yield:

: 444200-04-8
(4S)-4-benzyl-3-{(2S,3R)-3-(methoxymethoxy)-2-methyl-5-[(triisopropylsilyl)oxy]pentanoyl}-1,3-oxazolidin-2-one

: 444200-23-1
Toluene-4-sulfonic acid (2R,3R)-3-methoxymethoxy-2-methyl-5-triisopropylsilanyloxy-pentyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / sodium borohydride / tetrahydrofuran; H₂O / 0 - 20 °C

2: 88 percent / pyridine / 2 h / 0 °C

With pyridine; sodium tetrahydroborate; In tetrahydrofuran; water;
DOI:10.1021/ol026040k