2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Base Information

Chemical Name:2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate
CAS No.:773145-62-3
Molecular Formula:C₆₃H₅₀Cl₃NO₁₈
Molecular Weight:1215.44
Hs Code.:

Synonyms:2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Suppliers and Price of 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

There total 4 articles about 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-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:

: 13673-76-2
O¹,O²,O³,O⁴-tetrabenzoyl-O⁶-(tetra-O-benzoyl-α-D-galactopyranosyl)-ξ-D-glucopyranose

: 773145-62-3
2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 3 steps

1: HBr; AcOH / CH₂Cl₂ / 4 °C

2: aq. Ag₂CO₃ / acetone / 96 h / 20 °C

3: 2.29 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂

With hydrogen bromide; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; silver carbonate; In dichloromethane; acetone;
DOI:10.1248/cpb.52.965

Reference yield:

: 98-88-4
benzoyl chloride

: 773145-62-3
2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 20 - 80 °C

2: HBr; AcOH / CH₂Cl₂ / 4 °C

3: aq. Ag₂CO₃ / acetone / 96 h / 20 °C

4: 2.29 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂

With pyridine; hydrogen bromide; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; silver carbonate; In dichloromethane; acetone;
DOI:10.1248/cpb.52.965

Reference yield:

: 851078-70-1
C₆₁H₄₉BrO₁₇

: 773145-62-3
2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 2 steps

1: aq. Ag₂CO₃ / acetone / 96 h / 20 °C

2: 2.29 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂

With 1,8-diazabicyclo[5.4.0]undec-7-ene; silver carbonate; In dichloromethane; acetone;
DOI:10.1248/cpb.52.965