1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

Base Information

• Chemical Name: 1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol
• CAS No.: 256922-21-1
• Molecular Formula: C₄₆H₅₈O₇
• Molecular Weight: 722.962
• Mol file: 256922-21-1.mol

Synonyms:1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

Chemical Property of 1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

There total 1 articles about 1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol 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: 98.0%

1-bromo-octane (111-83-1) + 1D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol (154372-20-0) → 1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol (256922-21-1)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; for 24h;

DOI:10.1016/S0008-6215(99)00170-6

Reference yield:

1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol (256922-21-1) → 1-D-6-O-propenyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

Guidance literature:

With potassium tert-butylate; In dimethyl sulfoxide; at 60 ℃; for 1h;

DOI:10.1016/S0008-6215(99)00170-6

Reference yield:

1-D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol (256922-21-1) → 1-D-6-O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol

Guidance literature:

Multi-step reaction with 3 steps

1: tBuOK / dimethylsulfoxide / 1 h / 60 °C

2: aq. HCl / acetone / 10 h / Heating

3: zirconocene dichloride; silver perchlorate; 1,1,3,3-tetramethylurea / diethyl ether / 0 °C

With hydrogenchloride; zirconocene dichloride; potassium tert-butylate; silver perchlorate; tetramethylurea; In diethyl ether; dimethyl sulfoxide; acetone; 1: Isomerization / 2: dealkylation / 3: Substitution;

DOI:10.1016/S0008-6215(99)00170-6

upstream raw materials:

1-bromo-octane

1D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol

Downstream raw materials:

1-D-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-octyl-myo-inositol