ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
CAS No.:866885-62-3
Molecular Formula:C₅₀H₄₅NO₁₅S
Molecular Weight:931.971
Hs Code.:

Synonyms:ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

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Chemical Property of ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

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Technology Process of ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

There total 4 articles about ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-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: 95.0%

: 866885-61-2
ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-6-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

: 866885-62-3
ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: With triethylamine trihydrofluoride; In dichloromethane; for 144h;
DOI:10.1081/CAR-200066935

Reference yield:

: 866885-60-1
ethyl 6-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

: 866885-62-3
ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / silver(I) trifluoromethanesulfonate; molecular sieves 4 Angstroem / CH₂Cl₂ / 0.75 h / -55 °C

2: 95 percent / triethylamine trihydrofluoride / CH₂Cl₂ / 144 h

With 4 A molecular sieve; triethylamine trihydrofluoride; silver trifluoromethanesulfonate; In dichloromethane;
DOI:10.1081/CAR-200066935

Reference yield:

: 61198-88-7
2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl bromide

: 866885-62-3
ethyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / silver(I) trifluoromethanesulfonate; molecular sieves 4 Angstroem / CH₂Cl₂ / 0.75 h / -55 °C

2: 95 percent / triethylamine trihydrofluoride / CH₂Cl₂ / 144 h

With 4 A molecular sieve; triethylamine trihydrofluoride; silver trifluoromethanesulfonate; In dichloromethane;
DOI:10.1081/CAR-200066935