allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

Base Information

Chemical Name:allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside
CAS No.:640722-53-8
Molecular Formula:C₆₂H₆₂O₂₄
Molecular Weight:1191.16
Hs Code.:

Synonyms:allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

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Chemical Property of allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

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Technology Process of allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

There total 6 articles about allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside 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%

: 640722-52-7
C₆₉H₆₆O₂₄

: 640722-53-8
allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

Guidance literature:: With acetic acid; for 2h; Heating;
DOI:10.1016/j.carres.2003.08.004

Reference yield:

: 149707-75-5
2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl trichloroacetimidate

: 640722-53-8
allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1: 95 percent / TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

2: 96 percent / pyridine / 4 h / 20 °C

3: 85 percent / NIS; TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

4: 89 percent / DBU / CH₂Cl₂ / 3 h / 20 °C

5: 86 percent / TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

6: 87 percent / aq. AcOH / 2 h / Heating

With pyridine; N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane;
DOI:10.1016/j.carres.2003.08.004

Reference yield:

: isopropyl 4,6-O-benzylidene-1-deoxy-1-thio-β-D-glucopyranoside

: 640722-53-8
allyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-acetyl-β-D-glucopyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1: 95 percent / TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

2: 96 percent / pyridine / 4 h / 20 °C

3: 85 percent / NIS; TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

4: 89 percent / DBU / CH₂Cl₂ / 3 h / 20 °C

5: 86 percent / TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

6: 87 percent / aq. AcOH / 2 h / Heating

With pyridine; N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane;
DOI:10.1016/j.carres.2003.08.004