(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

Base Information

Chemical Name:(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone
CAS No.:1447732-00-4
Molecular Formula:C₂₇H₄₃NO₄Si
Molecular Weight:473.728
Hs Code.:

Synonyms:(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

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Chemical Property of (2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

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Technology Process of (2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

There total 4 articles about (2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-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: 99.0%

: 1447731-99-8
(2'R,3'S,4R,4'S,6E)-3-[(3-hydroxy-2,4,6-trimethyl-1-oxooct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

: 69739-34-0
t-butyldimethylsiyl triflate

: 1447732-00-4
(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; Inert atmosphere;
DOI:10.1016/j.tet.2013.06.012

Reference yield:

: 101711-78-8,131685-53-5
(3R)-3-propionyl-4-benzyloxazolidin-2-one

: 1447732-00-4
(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1.1: di-n-butylboryl trifluoromethanesulfonate; triethylamine / dichloromethane / 0 - 3 °C / Inert atmosphere

1.2: -65 °C / Inert atmosphere; Cooling with ice

2.1: 2,6-dimethylpyridine / dichloromethane / 4 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; di-n-butylboryl trifluoromethanesulfonate; triethylamine; In dichloromethane;
DOI:10.1021/ol3026457

Reference yield:

: 603121-10-4
(2S,4E)-2,4-dimethyl-4-hexenal

: 1447732-00-4
(2'R,3'S,4'S,6E,4R)-3-[(3-[tert-butyldimethylsilyloxy]-2,4,6-trimethyl-1-oxo-oct-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1.1: di-n-butylboryl trifluoromethanesulfonate; triethylamine / dichloromethane / 0 - 3 °C / Inert atmosphere

1.2: -65 °C / Inert atmosphere; Cooling with ice

2.1: 2,6-dimethylpyridine / dichloromethane / 4 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; di-n-butylboryl trifluoromethanesulfonate; triethylamine; In dichloromethane;
DOI:10.1021/ol3026457