(2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol

Base Information

• Chemical Name: (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol
• CAS No.: 182167-84-6
• Molecular Formula: C₂₅H₃₂O₈
• Molecular Weight: 460.524
• Mol file: 182167-84-6.mol

Synonyms:(2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol

Chemical Property of (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol

There total 3 articles about (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol 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: 82.0%

(3aS,4S,6R,7R,7aS)-4-Allyloxy-7-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran (182167-83-5) → (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol (182167-84-6)

Guidance literature:

With acetic acid; at 60 ℃; for 0.75h;

DOI:10.1080/07328309608005684

Reference yield:

allyl 2,3-O-isopropylidene-α-D-mannopyranoside (85207-16-5) → (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol (182167-84-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 86 percent / NaH / dimethylformamide / 2 h / Ambient temperature

2: 82 percent / 80percent aq. AcOH / 0.75 h / 60 °C

With sodium hydride; acetic acid; In N,N-dimethyl-formamide;

DOI:10.1080/07328309608005684

Reference yield:

p-methoxybenzyl chloride (824-94-2) → (2S,3S,4R,5S,6R)-2-Allyloxy-5-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-3,4-diol (182167-84-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 86 percent / NaH / dimethylformamide / 2 h / Ambient temperature

2: 82 percent / 80percent aq. AcOH / 0.75 h / 60 °C

With sodium hydride; acetic acid; In N,N-dimethyl-formamide;

DOI:10.1080/07328309608005684

upstream raw materials:

(3aS,4S,6R,7R,7aS)-4-Allyloxy-7-(4-methoxy-benzyloxy)-6-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran

allyl 2,3-O-isopropylidene-α-D-mannopyranoside

p-methoxybenzyl chloride

Downstream raw materials:

Allyl 2-O-benzoyl-3-O-[4-O-benzoyl-3,6-dideoxy-2-O-(p-methoxybenzyl)-α-D-xylo-hexopyranosyl]-4,6-di-O-(p-methoxybenzyl)-α-D-mannopyranoside

Allyl 2-O-benzoyl-3-O-[2,4-di-O-benzoyl-3,6-dideoxy-4-O-(p-methoxybenzyl)-α-D-arabino-hexopyranosyl]-4,6-di-O-(p-methoxybenzyl)-α-D-mannopyranoside

Allyl 2-O-benzoyl-3-O-(2,4-di-O-benzoyl-3,6-dideoxy-α-D-arabino-hexopyranosyl)-α-D-mannopyranoside

Allyl 2-O-benzoyl-3-O-(4-O-benzoyl-3,6-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside