methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

Base Information

Chemical Name:methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside
CAS No.:211806-82-5
Molecular Formula:C₃₀H₃₄O₆S
Molecular Weight:523.651
Hs Code.:

Synonyms:methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

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Technology Process of methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

There total 6 articles about methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside 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: 85.0%

: 3908-55-2
Trimethyl(methylthio)silane

: 211806-81-4
1,2-di-O-acetyl-3,4,6-tri-O-benzyl-β-D-(1-13C)-galactopyranose

: 211806-82-5
methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

Guidance literature:: With trimethylsilyl methanesulfonate; In dichloromethane;
DOI:10.1016/S0008-6215(98)00047-0

Reference yield:

: C₁₁⁽¹³⁾CH₂₀O₈

: 211806-82-5
methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

Guidance literature:: Multi-step reaction with 3 steps

2: 8 h / Heating

3: 85 percent / Me₃SiOSO₂Me / CH₂Cl₂

With trimethylsilyl methanesulfonate; In dichloromethane;
DOI:10.1016/S0008-6215(98)00047-0

Reference yield:

: C₁₃⁽¹³⁾CH₁₉BrO₉

: 211806-82-5
methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-(1-13C)-galactopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: Bu₄NBr, 2,4,6-trimethylpyridine / CH₂Cl₂ / 96 h / 23 °C

2: NaH / dimethylformamide

4: 8 h / Heating

5: 85 percent / Me₃SiOSO₂Me / CH₂Cl₂

With 2,4,6-trimethyl-pyridine; trimethylsilyl methanesulfonate; tetrabutylammomium bromide; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(98)00047-0