benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

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Chemical Name:benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside
CAS No.:88509-66-4
Molecular Formula:C₆₇H₇₄O₁₆
Molecular Weight:1135.31
Hs Code.:

Synonyms:benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

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Chemical Property of benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

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Technology Process of benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

There total 4 articles about benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-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: 77.0%

: 88509-65-3
benzyl 2,4-di-O-benzyl-3-O-(2,4-di-O-acetyl-3,6-di-O-benzyl-α-D-mannopyranosyl)-6-O-(2,6-di-O-acetyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

: 88509-66-4
benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

Guidance literature:: With sodium methylate; In methanol; Ambient temperature;
DOI:10.1016/0008-6215(83)88003-3

Reference yield:

: 69401-46-3
benzyl 2,4-di-O-benzyl-α-D-mannopyranoside

: 88509-66-4
benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 37 percent / silver triflate, 2,4,6-trimethylpyridine, 3 Angstroem molecular sieves / CH₂Cl₂ / -25 - 25 °C

2: 59 percent / silver triflate, 2,4,6-trimethylpyridine, 3 Angstroem molecular sieves / CH₂Cl₂ / -25 - 25 °C

3: 77 percent / sodium methoxide / methanol / Ambient temperature

With 2,4,6-trimethyl-pyridine; 3 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(83)88003-3

Reference yield:

: 88509-64-2
benzyl 2,4-di-O-benzyl-6-O-(2,6-di-O-acetyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

: 88509-66-4
benzyl 2,4-di-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,6-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / silver triflate, 2,4,6-trimethylpyridine, 3 Angstroem molecular sieves / CH₂Cl₂ / -25 - 25 °C

2: 77 percent / sodium methoxide / methanol / Ambient temperature

With 2,4,6-trimethyl-pyridine; 3 A molecular sieve; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(83)88003-3