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4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate

Base Information
  • Chemical Name:4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate
  • CAS No.:1143516-30-6
  • Molecular Formula:C29H32O9S
  • Molecular Weight:556.634
  • Hs Code.:
4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate

Synonyms:4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate

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Chemical Property of 4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate
Chemical Property:
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Technology Process of 4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate

There total 13 articles about 4,6,7-tri-O-benzyl-2,5-O-methylene-D-glycero-D-manno-heptitol-1,3-cyclic sulfate 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:
With ruthenium trichloride; sodium periodate; In tetrachloromethane; water; acetonitrile; at 20 ℃; for 2h;
Guidance literature:
Multi-step reaction with 12 steps
1.1: sodium hydroxide / water
2.1: methanol; toluene-4-sulfonic acid / 2 h / 70 °C
3.1: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 0 °C / Inert atmosphere
4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 °C
4.2: 0 - 20 °C
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 h / 20 °C
6.1: sodium hydrogencarbonate; Dess-Martin periodane / 0.25 h / 20 °C
7.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
7.2: -78 - 20 °C
8.1: AD-mix-β / water; tert-butyl alcohol / 168 h / 0 °C
9.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / Cooling with ice bath
9.2: 0 - 20 °C
10.1: methanol; toluene-4-sulfonic acid / 24 h / 20 °C
11.1: thionyl chloride; triethylamine / dichloromethane / 0.75 h / Cooling with ice bath
12.1: sodium periodate / ruthenium trichloride / tetrachloromethane; water; acetonitrile / 2 h / 20 °C
With 1H-imidazole; methanol; sodium hydroxide; sodium periodate; n-butyllithium; thionyl chloride; AD-mix-β; tetrabutyl ammonium fluoride; sodium hydride; sodium hydrogencarbonate; Dess-Martin periodane; toluene-4-sulfonic acid; triethylamine; ruthenium trichloride; In tetrahydrofuran; tetrachloromethane; hexane; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; mineral oil; tert-butyl alcohol;
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride; triethylamine / dichloromethane / 0.75 h / Cooling with ice bath
2: sodium periodate / ruthenium trichloride / tetrachloromethane; water; acetonitrile / 2 h / 20 °C
With sodium periodate; thionyl chloride; triethylamine; ruthenium trichloride; In tetrachloromethane; dichloromethane; water; acetonitrile;
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