(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

Base Information

Chemical Name:(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one
CAS No.:175853-64-2
Molecular Formula:C₂₁H₂₂BrNO₃
Molecular Weight:416.315
Hs Code.:

Synonyms:(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

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Chemical Property of (R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

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Technology Process of (R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

There total 8 articles about (R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-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:

: 1775-44-6,10321-71-8,16666-43-6
(2E)-4-methylpent-2-enoic acid

: 175853-64-2
(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran

2: 1.) n-butyllithium / 1.) THF, hexane, 10 min, 2.) THF, hexane

3: 80 percent / CuBr₂*SMe₂ / tetrahydrofuran

4: 1.) diisopropylethylamine, dibutylboron triflate, 2.) N-bromosuccinimide / 1.) CH₂Cl₂, 2.) CH₂Cl₂

With N-Bromosuccinimide; n-butyllithium; copper bromide dimethyl sulfide complex; di-n-butylboryl trifluoromethanesulfonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4020(97)10127-2

Reference yield:

: 100-58-3
phenylmagnesium bromide

: 175853-64-2
(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / CuBr₂*SMe₂ / tetrahydrofuran

2: 1.) diisopropylethylamine, dibutylboron triflate, 2.) N-bromosuccinimide / 1.) CH₂Cl₂, 2.) CH₂Cl₂

With N-Bromosuccinimide; copper bromide dimethyl sulfide complex; di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4020(97)10127-2

Reference yield:

: 194031-58-8
(4R,2E)-3-(1-oxo-2-isohexenyl)-4-phenyl-2-oxazolidinone

: 175853-64-2
(R)-3-((2R,3R)-2-Bromo-4-methyl-3-phenyl-pentanoyl)-4-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / CuBr₂*SMe₂ / tetrahydrofuran

2: 1.) diisopropylethylamine, dibutylboron triflate, 2.) N-bromosuccinimide / 1.) CH₂Cl₂, 2.) CH₂Cl₂

With N-Bromosuccinimide; copper bromide dimethyl sulfide complex; di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4020(97)10127-2