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2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate

Base Information
  • Chemical Name:2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate
  • CAS No.:82462-51-9
  • Molecular Formula:C25H30O7Si
  • Molecular Weight:470.595
  • Hs Code.:
2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate

Synonyms:2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate

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Chemical Property of 2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate
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Technology Process of 2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate

There total 3 articles about 2-(trimethylsilyl)ethyl 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonoate 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:
Guidance literature:
Multi-step reaction with 2 steps
1: 73 percent / 1.) 2-chloro-N-methylpyridinium iodide, triethylamine / acetonitrile / Ambient temperature; 1.) 1.5 h, 2.) overnight
2: 22 percent / H2 / 10percent Pd-C / ethanol / 48 h / 760 Torr
With 2-chloro-1-methyl-pyridinium iodide; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; acetonitrile;
DOI:10.1039/P19850000621
Guidance literature:
Multi-step reaction with 2 steps
1: 73 percent / 1.) 2-chloro-N-methylpyridinium iodide, triethylamine / acetonitrile / Ambient temperature; 1.) 1.5 h, 2.) overnight
2: 22 percent / H2 / 10percent Pd-C / ethanol / 48 h / 760 Torr
With 2-chloro-1-methyl-pyridinium iodide; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; acetonitrile;
DOI:10.1039/P19850000621
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