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C32H36N4O18

Base Information
  • Chemical Name:C32H36N4O18
  • CAS No.:1365254-67-6
  • Molecular Formula:C32H36N4O18
  • Molecular Weight:764.654
  • Hs Code.:
C<sub>32</sub>H<sub>36</sub>N<sub>4</sub>O<sub>18</sub>

Synonyms:C32H36N4O18

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Chemical Property of C32H36N4O18
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Technology Process of C32H36N4O18

There total 5 articles about C32H36N4O18 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: 51.0%

Guidance literature:
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 3h;
DOI:10.1016/j.tet.2012.01.080
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogenchloride / water; ethyl acetate / 10 h / 20 °C / Inert atmosphere
2: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 10 h / 20 °C / Inert atmosphere
3: osmium(VIII) oxide; 4-methylmorpholine N-oxide; hydroquinidein 1,4-phthalazinediyl diether / tetrahydrofuran; water; tert-butyl alcohol / 20 °C / Inert atmosphere
4: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 20 °C
With 4-methyl-morpholine; hydrogenchloride; osmium(VIII) oxide; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 4-methylmorpholine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; hydroquinidein 1,4-phthalazinediyl diether; In tetrahydrofuran; methanol; water; ethyl acetate; tert-butyl alcohol; 3: Sharpless asymmetric dihydroxylation;
DOI:10.1016/j.tet.2012.01.080
Guidance literature:
Multi-step reaction with 3 steps
1: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 10 h / 20 °C / Inert atmosphere
2: osmium(VIII) oxide; 4-methylmorpholine N-oxide; hydroquinidein 1,4-phthalazinediyl diether / tetrahydrofuran; water; tert-butyl alcohol / 20 °C / Inert atmosphere
3: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 20 °C
With 4-methyl-morpholine; osmium(VIII) oxide; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 4-methylmorpholine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; hydroquinidein 1,4-phthalazinediyl diether; In tetrahydrofuran; methanol; water; tert-butyl alcohol; 2: Sharpless asymmetric dihydroxylation;
DOI:10.1016/j.tet.2012.01.080
upstream raw materials:

C46H44N4O14

C15H23NO6

C26H38N2O12

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