1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

Base Information

Chemical Name:1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose
CAS No.:119803-53-1
Molecular Formula:C₃₃H₃₇Cl₃O₁₉
Molecular Weight:844.004
Hs Code.:

Synonyms:1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

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Chemical Property of 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

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Technology Process of 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

There total 5 articles about 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose 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: 97.0%

: 119803-52-0
1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-α-D-galactopyranosyl)-β-D-glucopyranose

: 76-02-8
trifluoroacetyl chloride

: 119803-53-1
1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

Guidance literature:: With pyridine; In dichloromethane; 0 deg C, , 30 min, RT, 3 h;

Reference yield:

: 54769-36-7
N-benzoyloxybenzotriazole

: 119803-53-1
1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / triethylamine / CH₂Cl₂ / 24 h / Ambient temperature

2: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

3: 51 percent / sodium nitrite / dimethylformamide / 3 h / Ambient temperature

4: 97 percent / pyridine / CH₂Cl₂ / 0 deg C, , 30 min, RT, 3 h

With pyridine; triethylamine; sodium nitrite; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 72718-62-8,81661-67-8,102281-77-6,120852-02-0,93417-43-7
1,2,3,6-tetra-O-acetyl-4-O-(2',3'-di-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside

: 119803-53-1
1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / triethylamine / CH₂Cl₂ / 24 h / Ambient temperature

2: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

3: 51 percent / sodium nitrite / dimethylformamide / 3 h / Ambient temperature

4: 97 percent / pyridine / CH₂Cl₂ / 0 deg C, , 30 min, RT, 3 h

With pyridine; triethylamine; sodium nitrite; In dichloromethane; N,N-dimethyl-formamide;