phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside
CAS No.:1352299-30-9
Molecular Formula:C₅₀H₄₂F₁₃NO₁₀S
Molecular Weight:1095.93
Hs Code.:

Synonyms:phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

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Chemical Property of phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

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Technology Process of phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

There total 6 articles about phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside 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:

: C₄₃H₄₃NO₉S

: 52447-22-0
perfluoroheptanoyl chloride

: 1352299-30-9
phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

Guidance literature:: With triethylamine; In tetrahydrofuran; water; at 0 - 20 ℃; for 2h;
DOI:10.1016/j.tet.2011.09.030

Reference yield:

: phenyl 2,3,-di-O-benzoyl-4-O-benzyl-1-thio-β-D-glucopyranoside

: 1352299-30-9
phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: tributylphosphine; 1,1'-azodicarbonyl-dipiperidine / tetrahydrofuran / 18 h / 60 °C / Inert atmosphere

2: sodium azide; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 h / 60 °C / Inert atmosphere

3: ammonium chloride; zinc / tetrahydrofuran; water / 0.17 h / 0 - 20 °C

4: triethylamine / tetrahydrofuran; water / 2 h / 0 - 20 °C

With sodium azide; tributylphosphine; tetra-(n-butyl)ammonium iodide; ammonium chloride; triethylamine; zinc; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2011.09.030

Reference yield:

: 1352299-28-5
phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-{4-[2-(2-chloroethoxy)ethoxy]phenyl}-1-thio-β-D-glucopyranoside

: 1352299-30-9
phenyl 2,3-O-di-benzoyl-4-O-benzyl-6-O-(4-(2-(2-tridecafluorohexanecarboxamido)ethoxy)ethoxy)phenyl-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: sodium azide; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 h / 60 °C / Inert atmosphere

2: ammonium chloride; zinc / tetrahydrofuran; water / 0.17 h / 0 - 20 °C

3: triethylamine / tetrahydrofuran; water / 2 h / 0 - 20 °C

With sodium azide; tetra-(n-butyl)ammonium iodide; ammonium chloride; triethylamine; zinc; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2011.09.030