octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

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Chemical Name:octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside
CAS No.:900523-85-5
Molecular Formula:C₅₆H₆₈O₁₁
Molecular Weight:917.149
Hs Code.:

Synonyms:octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

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Chemical Property of octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

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Technology Process of octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

There total 4 articles about octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside 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: 84.0%

: 900523-83-3
octyl 3,5-di-O-benzyl-α-D-arabinofuranoside

: 130525-72-3
ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

: 900523-85-5
octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; at -40 - 20 ℃; for 3.5h;
DOI:10.1139/V06-049

Reference yield:

: 900523-84-4
octyl 2,3-anhydro-5-O-benzyl-α-D-lyxofuranoside

: 900523-85-5
octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / phenylmethanol / 100 °C

2: 84 percent / molecular sieves 4 Angstroem; N-iodosuccinimide; silver triflate / CH₂Cl₂ / 3.5 h / -40 - 20 °C

With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; benzyl alcohol;
DOI:10.1139/V06-049

Reference yield:

: 100-39-0
benzyl bromide

: 900523-85-5
octyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / NaH / tetrahydrofuran / 2 h / 0 - 20 °C

2: 88 percent / phenylmethanol / 100 °C

3: 84 percent / molecular sieves 4 Angstroem; N-iodosuccinimide; silver triflate / CH₂Cl₂ / 3.5 h / -40 - 20 °C

With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; sodium hydride; In tetrahydrofuran; dichloromethane; benzyl alcohol;
DOI:10.1139/V06-049