octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

Base Information

Chemical Name:octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside
CAS No.:849208-14-6
Molecular Formula:C₅₆H₇₀O₁₁
Molecular Weight:919.165
Hs Code.:

Synonyms:octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

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Chemical Property of octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

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Technology Process of octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

There total 6 articles about octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 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:

: [(2R,3R,4S,5S,6S)-3,4-Bis-benzyloxy-5-methoxy-6-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-octyloxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-2-ylmethoxy]-tert-butyl-diphenyl-silane

: 849208-14-6
octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 48h;
DOI:10.1016/j.tetasy.2004.11.063

Reference yield:

: 849208-12-4
octyl 3,4-di-O-benzyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

: 849208-14-6
octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / imidazole / dimethylformamide / 20 °C

2: sodium hydride / dimethylformamide / 0 - 20 °C

3: 310 mg / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 48 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2004.11.063

Reference yield:

: 849208-13-5
octyl 3,4-di-O-benzyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

: 849208-14-6
octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / dimethylformamide / 0 - 20 °C

2: 310 mg / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 48 h / 20 °C

With tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2004.11.063