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

Base Information

• Chemical Name: octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside
• CAS No.: 569659-42-3
• Molecular Formula: C₄₆H₅₀O₁₃
• Molecular Weight: 810.895

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

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

Chemical Property:

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

There total 3 articles about octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-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: 88.0%

octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-5-O-tert-butyldiphenylsilyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside (569659-41-2) → octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside (569659-42-3)

Guidance literature:

With n-Bu₄F*3H₂O; In tetrahydrofuran; at 20 ℃; for 4h;

DOI:10.1016/S0008-6215(02)00541-4

Reference yield:

p-cresyl 2,3-di-O-benzoyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside (204918-56-9) → octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside (569659-42-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 82 percent / N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.5 h / 0 °C

2: 88 percent / n-Bu₄F*3H₂O / tetrahydrofuran / 4 h / 20 °C

With N-iodo-succinimide; n-Bu₄F*3H₂O; silver trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane;

DOI:10.1016/S0008-6215(02)00541-4

Reference yield:

octyl 2,3-di-O-benzoyl-α-D-arabinofuranoside (329360-19-2) → octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside (569659-42-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 82 percent / N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.5 h / 0 °C

2: 88 percent / n-Bu₄F*3H₂O / tetrahydrofuran / 4 h / 20 °C

With N-iodo-succinimide; n-Bu₄F*3H₂O; silver trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane;

DOI:10.1016/S0008-6215(02)00541-4

upstream raw materials:

octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-5-O-tert-butyldiphenylsilyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside

p-cresyl 2,3-di-O-benzoyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

octyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Downstream raw materials:

octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-(5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl))-α-D-arabinofuranoside

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