3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

Base Information

Chemical Name:3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate
CAS No.:666727-80-6
Molecular Formula:C₄₄H₄₀Cl₃NO₁₄
Molecular Weight:913.159
Hs Code.:

Synonyms:3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

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Chemical Property of 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

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Technology Process of 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

There total 9 articles about 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate 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: 81.0%

: 545-06-2
trichloroacetonitrile

: 666727-75-9
allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside

: 666727-80-6
3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside; palladium dichloride; In methanol; at 40 ℃; for 4h;

trichloroacetonitrile; With potassium carbonate; In dichloromethane; at 20 ℃;
DOI:10.1016/j.carres.2005.01.015

Reference yield:

: 93382-48-0
allyl 4,6-O-benzylidene-α-D-glucopyranoside

: 666727-80-6
3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 80 percent / pyridine / 20 °C

2.1: 95 percent / pyridine / 20 °C

3.1: PdCl₂ / methanol / 4 h / 40 °C

3.2: 80 percent / K₂CO₃ / CH₂Cl₂ / 20 °C

4.1: 53 percent / TMSOTf / CH₂Cl₂ / 3 h / 0 - 20 °C

5.1: PdCl₂ / methanol / 4 h / 40 °C

5.2: 81 percent / K₂CO₃ / CH₂Cl₂ / 20 °C

With pyridine; trimethylsilyl trifluoromethanesulfonate; palladium dichloride; In methanol; dichloromethane;
DOI:10.1016/j.carres.2005.01.015

Reference yield:

: 98-88-4
benzoyl chloride

: 666727-80-6
3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 80 percent / pyridine / 20 °C

2.1: 95 percent / pyridine / 20 °C

3.1: PdCl₂ / methanol / 4 h / 40 °C

3.2: 80 percent / K₂CO₃ / CH₂Cl₂ / 20 °C

4.1: 53 percent / TMSOTf / CH₂Cl₂ / 3 h / 0 - 20 °C

5.1: PdCl₂ / methanol / 4 h / 40 °C

5.2: 81 percent / K₂CO₃ / CH₂Cl₂ / 20 °C

With pyridine; trimethylsilyl trifluoromethanesulfonate; palladium dichloride; In methanol; dichloromethane;
DOI:10.1016/j.carres.2005.01.015