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Technology Process of 5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

Base Information
  • Chemical Name:5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose
  • CAS No.:1046825-05-1
  • Molecular Formula:C59H52O20
  • Molecular Weight:1081.05
  • Hs Code.:
5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

Synonyms:5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

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Chemical Property of 5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose
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Technology Process of 5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

There total 1 articles about 5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose 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: 94.0%

C<sub>66</sub>H<sub>58</sub>O<sub>20</sub>
1046825-12-0

C66H58O20

5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose
1046825-05-1

5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

Guidance literature:
With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate; at 20 ℃; for 18h; under 750.075 Torr;
DOI:10.1039/b803409e

Reference yield: 92.0%

5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose
1046825-05-1

5-O-acetyl-[2,3,5-tri-O-benzoyl-α-D-(1->2)-arabinofuranosyl]-[2,3,5-tri-O-benzoyl-α-D-(1->3)-arabinofuranosyl]-D-arabinofuranose

trichloroacetonitrile
545-06-2

trichloroacetonitrile

C<sub>61</sub>H<sub>52</sub>Cl<sub>3</sub>NO<sub>20</sub>
1046825-06-2

C61H52Cl3NO20

Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at -10 ℃; for 0.333333h;
DOI:10.1039/b803409e
upstream raw materials:

C66H58O20

Downstream raw materials:

C61H52Cl3NO20

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