(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

Base Information

Chemical Name:(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one
CAS No.:126788-91-8
Molecular Formula:C₃₂H₃₇NO₇
Molecular Weight:547.648
Hs Code.:

Synonyms:(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

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Chemical Property of (4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

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Technology Process of (4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

There total 5 articles about (4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-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:

: 100-39-0
benzyl bromide

: 126788-91-8
(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / NaH / dimethylformamide; diethyl ether / 1.) 0 deg C, 20 min, 2.) RT, 12 h

2: 89 percent / 0.15 M OsO₄, KIO₄ / acetone; H₂O / 6 h / Ambient temperature

3: 1.) triethylamine, di-n-butylboron triflate / 1.) CH₂Cl₂, -50 deg C, 90 min, 2.) -40 deg C, 1 h

With osmium(VIII) oxide; potassium metaperiodate; di-n-butylboryl trifluoromethanesulfonate; sodium hydride; triethylamine; In diethyl ether; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja00164a023

Reference yield:

: 126788-88-3
(R)-1-((2-methylpent-4-enyloxy)methyl)benzene

: 126788-91-8
(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / 0.15 M OsO₄, KIO₄ / acetone; H₂O / 6 h / Ambient temperature

2: 1.) triethylamine, di-n-butylboron triflate / 1.) CH₂Cl₂, -50 deg C, 90 min, 2.) -40 deg C, 1 h

With osmium(VIII) oxide; potassium metaperiodate; di-n-butylboryl trifluoromethanesulfonate; triethylamine; In water; acetone;
DOI:10.1021/ja00164a023

Reference yield:

: 63501-27-9
(2R)-2-methyl-4-penten-1-ol

: 126788-91-8
(4R,5S)-3-[(2R,3S,5R)-6-Benzyloxy-3-hydroxy-2-(4-methoxy-benzyloxy)-5-methyl-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / NaH / dimethylformamide; diethyl ether / 1.) 0 deg C, 20 min, 2.) RT, 12 h

2: 89 percent / 0.15 M OsO₄, KIO₄ / acetone; H₂O / 6 h / Ambient temperature

3: 1.) triethylamine, di-n-butylboron triflate / 1.) CH₂Cl₂, -50 deg C, 90 min, 2.) -40 deg C, 1 h

With osmium(VIII) oxide; potassium metaperiodate; di-n-butylboryl trifluoromethanesulfonate; sodium hydride; triethylamine; In diethyl ether; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja00164a023