octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

Base Information

• Chemical Name: octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside
• CAS No.: 1240385-88-9
• Molecular Formula: C₅₀H₆₀O₁₂
• Molecular Weight: 853.019

Synonyms:octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

Chemical Property of octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

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Technology Process of octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

There total 1 articles about octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside 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: 87.0%

ethyl 3-O-acetyl-4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside (887478-25-3) + octyl 4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside (1240385-87-8) → octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside (1240385-88-9)

Guidance literature:

With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at 0 ℃; Inert atmosphere; Molecular sieve;

DOI:10.1016/j.carres.2010.04.006

Reference yield: 80.5%

octyl 3-O-cetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside (1240385-88-9) → octyl 4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside (1240385-89-0)

Guidance literature:

With methanol; acetyl chloride; In dichloromethane; at 20 ℃; for 12h;

DOI:10.1016/j.carres.2010.04.006

upstream raw materials:

ethyl 3-O-acetyl-4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside

octyl 4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

Downstream raw materials:

octyl 4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

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