2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

Base Information

Chemical Name:2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate
CAS No.:154460-36-3
Molecular Formula:C₂₆H₂₄Cl₃NO₁₀
Molecular Weight:616.836
Hs Code.:

Synonyms:2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

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Chemical Property of 2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

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Technology Process of 2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

There total 11 articles about 2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl 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

: 2,3-di-O-benzoyl-4,6-O-<(R)-1-methoxycarbonylethylidene>-D-galactopyranose

: 154460-36-3
2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

Guidance literature:: With potassium carbonate; In dichloromethane; for 336h;
DOI:10.1016/0008-6215(94)80063-4

Reference yield: 66.0%

: 545-06-2
trichloroacetonitrile

: 2,3-di-O-benzoyl-4,6-O-<(R)-1-methoxycarbonylethylidene>-D-galactopyranose

: 2,3-di-O-benzoyl-4,6-O-<(R)-1-methoxycarbonylethylidene>-β-D-galactopyranosyl trichloroacetimidate

: 154460-36-3
2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

Guidance literature:: With potassium carbonate; In dichloromethane; for 96h;
DOI:10.1016/0008-6215(94)80063-4

Reference yield:

: 98-88-4
benzoyl chloride

: 154460-36-3
2,3-di-O-benzoyl-4,6-O-<1-(R)-methoxycarbonyl(ethylidene)>-α-D-galactopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / pyridine / 5 h / Ambient temperature

2: 76 percent / aq. AcOH / 1.5 h / 80 °C

3: 70 percent / BF₃*Et₂O / acetonitrile / 2 h / Ambient temperature

4: 43 percent / PdCl₂, 90percent aq. AcOH / 6 h / 60 °C

5: 66 percent / K₂CO₃ / CH₂Cl₂ / 96 h

With pyridine; boron trifluoride diethyl etherate; potassium carbonate; acetic acid; palladium dichloride; In dichloromethane; acetonitrile;
DOI:10.1016/0008-6215(94)80063-4