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3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol

Base Information
  • Chemical Name:3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol
  • CAS No.:170900-81-9
  • Molecular Formula:C42H44O7
  • Molecular Weight:660.807
  • Hs Code.:
3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol

Synonyms:3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol

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Chemical Property of 3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol
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Technology Process of 3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-myo-inositol

There total 10 articles about 3,4,5,6-tetra-O-benzyl-1-O-p-methoxybenzyl-D-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:
Guidance literature:
3,4,5,6-tetra-O-benzyl inositol; With di(n-butyl)tin oxide; In methanol; for 4h; Reflux; Inert atmosphere;
p-methoxybenzyl chloride; With tetrabutylammomium bromide; In N,N-dimethyl-formamide; toluene; at 0 - 80 ℃; Molecular sieve; Inert atmosphere;
DOI:10.1021/acs.joc.9b00126
Guidance literature:
With acetyl chloride; In methanol; at 20 ℃; Reagent/catalyst; Inert atmosphere;
DOI:10.1021/acs.joc.9b00126
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 0 °C / Inert atmosphere
1.2: 24 h / 20 °C / Inert atmosphere
2.1: water; acetic acid / 4 h / 100 °C
3.1: di(n-butyl)tin oxide / toluene / 18 h / 140 °C / Inert atmosphere
With water; sodium hydride; di(n-butyl)tin oxide; acetic acid; In N,N-dimethyl-formamide; toluene;
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