octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

Base Information

Chemical Name:octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside
CAS No.:685111-75-5
Molecular Formula:C₄₇H₅₂O₁₃
Molecular Weight:824.922
Hs Code.:

Synonyms:octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

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Chemical Property of octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

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Technology Process of octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

There total 5 articles about octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-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: 97.0%

: 569659-32-1
octyl 2,5-di-O-benzoyl-α-D-arabinofuranoside

: 685111-64-2
p-toluyl 2,3-di-O-benzoyl-5-O-methyl-1-thio-α-D-arabinofuranoside

: 685111-75-5
octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.0833333h;
DOI:10.1016/j.carres.2003.12.015

Reference yield:

: 204918-49-0
p-methylphenyl 1-thio-α-D-arabinofuranoside

: 685111-75-5
octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 5 steps

1: DMAP / pyridine; CH₂Cl₂ / 20 °C

2: 85 percent / pyridine / 20 °C

3: 86 percent / p-toluenesulfonic acid / methanol; CH₂Cl₂ / 20 °C

4: 76 percent / fluoroboric acid / hexane; CH₂Cl₂; H₂O / 1.83 h / 0 °C

5: 97 percent / N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.08 h / 0 °C

With pyridine; dmap; N-iodo-succinimide; tetrafluoroboric acid; silver trifluoromethanesulfonate; toluene-4-sulfonic acid; In pyridine; methanol; hexane; dichloromethane; water;
DOI:10.1016/j.carres.2003.12.015

Reference yield:

: 685111-68-6
p-toluyl 2,3-di-O-benzoyl-1-thio-α-D-arabinofuranoside

: 685111-75-5
octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->3)-2,5-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / fluoroboric acid / hexane; CH₂Cl₂; H₂O / 1.83 h / 0 °C

2: 97 percent / N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.08 h / 0 °C

With N-iodo-succinimide; tetrafluoroboric acid; silver trifluoromethanesulfonate; In hexane; dichloromethane; water;
DOI:10.1016/j.carres.2003.12.015