4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

Base Information

Chemical Name:4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside
CAS No.:866029-02-9
Molecular Formula:C₃₃H₃₈Cl₃NO₁₈
Molecular Weight:843.02
Hs Code.:

Synonyms:4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

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Chemical Property of 4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

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Technology Process of 4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

There total 1 articles about 4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside 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:

: 866028-98-0
1,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-α-D-mannopyranose

: 866029-02-9
4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / NH₂NH₂*HOAc / dimethylformamide / 4 h / 20 °C

2: 79 percent / DBU / CH₂Cl₂ / 1 h / -5 °C

With hydrazinium monoacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200500146

Reference yield: 55.0%

: 866029-02-9
4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

: 18968-05-3
1,3,4,6-tetra-O-acetyl-β-D-mannopyranose

: 866029-05-2
1,3,4,6-tetra-O-acetyl-2-O-[4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-α-D-mannopyranosyl]-β-D-mannopyranose

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 0 - 10 ℃; for 0.5h;
DOI:10.1002/ejoc.200500146

Reference yield:

: 866029-02-9
4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-1-O-trichloroacetimidoyl-α-D-mannopyranoside

: 3-aminopropyl 3,4,6-tri-O-acetyl-2-O-[4,6-di-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-O-benzoyl-α-D-mannopyranosyl]-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 55 percent / BF₃*OEt₂ / CH₂Cl₂ / 0.5 h / 0 - 10 °C

2: 85 percent / NH₂NH₂*HOAc / dimethylformamide / 2 h / 20 °C

3: 89 percent / K₂CO₃ / CH₂Cl₂ / 2 h / 20 °C

4: 91 percent / TMSOTf / CH₂Cl₂ / 1.5 h / 0 - 10 °C

5: H₂ / Pd/C / ethanol; acetic acid; ethyl acetate / 3 h / 20 °C / 760 Torr

With trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; hydrogen; hydrazinium monoacetate; potassium carbonate; palladium on activated charcoal; In ethanol; dichloromethane; acetic acid; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200500146