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N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane

Base Information Edit
  • Chemical Name:N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane
  • CAS No.:80958-68-5
  • Molecular Formula:C34H45N3O6S2
  • Molecular Weight:655.88
  • Hs Code.:
  • Mol file:80958-68-5.mol
N<sup>2</sup>,N<sup>12</sup>-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane

Synonyms:N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane

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Chemical Property of N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane Edit
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Technology Process of N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane

There total 4 articles about N2,N12-di-p-toluenesulfonyl-18-hydroxy-19-hydroxymethyl-18,19'-O-isopropylidene-2,12-diaza<13>(2,5)pyridinophane 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: thionyl chloride / benzene / Ambient temperature
2: 60 percent / dimethylformamide / 3 h / 90 °C
With thionyl chloride; In N,N-dimethyl-formamide; benzene;
DOI:10.1246/cl.1981.1749
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