benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

Base Information

Chemical Name:benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate
CAS No.:225640-48-2
Molecular Formula:C₃₆H₄₀O₆SSi
Molecular Weight:628.861
Hs Code.:

Synonyms:benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

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Chemical Property of benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

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Technology Process of benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

There total 5 articles about benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate 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: 100.0%

: 27607-77-8
trimethylsilyl trifluoromethanesulfonate

: 225640-46-0
benzyl (phenyl 2,3-di-O-benzyl-1-thio-β-D-galactopyranosid)uronate

: 225640-48-2
benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at -10 ℃; for 0.166667h;
DOI:10.1016/S0008-6215(98)00312-7

Reference yield:

: 100-39-0
benzyl bromide

: 225640-48-2
benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Bu₂SnO, 2.) Bu₄NI / 1.) toluene, reflux, 2.) toluene, 60 deg C, 3 h

2: 100 percent / 2,6-lutidine / CH₂Cl₂ / 0.17 h / -10 °C

With 2,6-dimethylpyridine; tetra-(n-butyl)ammonium iodide; di(n-butyl)tin oxide; In dichloromethane;
DOI:10.1016/S0008-6215(98)00312-7

Reference yield:

: 124476-97-7
phenyl 2-O-benzyl-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside

: 225640-48-2
benzyl (phenyl 2,3-di-O-benzyl-1-thio-4-O-trimethylsilyl-β-D-galactopyranosid)uronate

Guidance literature:: Multi-step reaction with 4 steps

1: 61 percent / Ac₂O, PDC / CH₂Cl₂ / 3 h / Ambient temperature; in dark

2: 98 percent / acetyl chloride / 2.5 h / 0 deg C then rt

3: 1.) Bu₂SnO, 2.) Bu₄NI / 1.) toluene, reflux, 2.) toluene, 60 deg C, 3 h

4: 100 percent / 2,6-lutidine / CH₂Cl₂ / 0.17 h / -10 °C

With 2,6-dimethylpyridine; dipyridinium dichromate; acetic anhydride; tetra-(n-butyl)ammonium iodide; di(n-butyl)tin oxide; acetyl chloride; In dichloromethane;
DOI:10.1016/S0008-6215(98)00312-7