methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside

Base Information

• Chemical Name: methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside
• CAS No.: 127258-11-1
• Molecular Formula: C₁₆H₂₂O₆
• Molecular Weight: 310.347
• Mol file: 127258-11-1.mol

Synonyms:methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside

Chemical Property of methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

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• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside

There total 1 articles about methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside 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:

p-Anisaldehyde dimethyl acetal (2186-92-7) + methyl 6-O-(tert-butyldimethylsilyl)-3-deoxy-3-methyl-α-D-idopyranoside (127258-09-7) → methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside (127258-11-1)

Guidance literature:

With camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; Yield given. Multistep reaction; 1.) benzene, reflux , 1h, 2.) THF, 6h, RT;

DOI:10.1021/jo00296a040

Reference yield: 87.0%

methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside (127258-11-1) → methyl 2,4-di-O-(4-methoxybenzylidene)-3,6-dideoxy-6-iodo-3-methyl-α-D-idopyranoside (127258-13-3)

Guidance literature:

With pyridine; iodine; triphenylphosphine; In benzene; at 45 ℃; for 44h;

DOI:10.1021/jo00296a040

Reference yield:

methyl 2,4-di-O-(4-methoxybenzylidene)-3-deoxy-3-methyl-α-D-idopyranoside (127258-11-1) → (2R,4S,5R,6R)-2-(4-methoxyphenyl)-5-methyl-6-vinyl-1,3-dioxane-4-carboxaldehyde (127258-14-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 87 percent / I₂, PPh₃, pyridine / benzene / 44 h / 45 °C

2: zinc-metal, pyridine / aq. ethanol / 0.17 h / Heating

With pyridine; iodine; triphenylphosphine; zinc; In ethanol; benzene;

DOI:10.1021/jo00296a040

upstream raw materials:

p-Anisaldehyde dimethyl acetal

methyl 6-O-(tert-butyldimethylsilyl)-3-deoxy-3-methyl-α-D-idopyranoside

Downstream raw materials:

methyl 2,4-di-O-(4-methoxybenzylidene)-3,6-dideoxy-6-iodo-3-methyl-α-D-idopyranoside

(2R,4S,5R,6R)-2-(4-methoxyphenyl)-5-methyl-6-vinyl-1,3-dioxane-4-carboxaldehyde

(2S,4S,5R,6R)-2-(4-methoxyphenyl)-5-methyl-6-vinyl-1,3-dioxane-4-carboxaldehyde