(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

Base Information

Chemical Name:(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester
CAS No.:311803-98-2
Molecular Formula:C₂₃H₂₇NO₆
Molecular Weight:413.47
Hs Code.:

Synonyms:(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

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Chemical Property of (S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

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Technology Process of (S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

There total 3 articles about (S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester 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: 75.0%

: 311803-97-1
(4R,5S)-3-(3-Furan-2-yl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one

: 5292-43-3
bromoacetic acid tert-butyl ester

: 311803-98-2
(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

Guidance literature:: (4R,5S)-3-(3-Furan-2-yl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;

bromoacetic acid tert-butyl ester; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2005.06.090

Reference yield:

: 10031-90-0
ethyl 3-(furan-2-yl)propanoate

: 311803-98-2
(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 100 percent / aq. LiOH / tetrahydrofuran; propan-2-ol

2.1: 66 percent / trimethylacetyl chloride; TEA; LiCl / tetrahydrofuran / 0 °C

3.1: LDA / tetrahydrofuran / -78 °C

3.2: 75 percent / tetrahydrofuran

With lithium hydroxide; TEA; pivaloyl chloride; lithium chloride; lithium diisopropyl amide; In tetrahydrofuran; isopropyl alcohol;
DOI:10.1016/j.bmcl.2005.06.090

Reference yield:

: 935-13-7
3-(2-furyl)propanoic acid

: 311803-98-2
(S)-3-Furan-2-ylmethyl-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 66 percent / trimethylacetyl chloride; TEA; LiCl / tetrahydrofuran / 0 °C

2.1: LDA / tetrahydrofuran / -78 °C

2.2: 75 percent / tetrahydrofuran

With TEA; pivaloyl chloride; lithium chloride; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2005.06.090