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N-(p-toluenesulfonyl)pyrrolo diazene

Base Information
  • Chemical Name:N-(p-toluenesulfonyl)pyrrolo diazene
  • CAS No.:152940-78-8
  • Molecular Formula:C13H13N3O2S
  • Molecular Weight:275.331
  • Hs Code.:
N-(p-toluenesulfonyl)pyrrolo diazene

Synonyms:N-(p-toluenesulfonyl)pyrrolo diazene

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Chemical Property of N-(p-toluenesulfonyl)pyrrolo diazene
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Technology Process of N-(p-toluenesulfonyl)pyrrolo diazene

There total 6 articles about N-(p-toluenesulfonyl)pyrrolo diazene 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 6 steps
1: 91 percent / Bu4NHSO4, KOH / CH2Cl2
2: 91 percent / DIBAL / CH2Cl2
3: 78 percent / Ph3PCl2 / CH2Cl2
4: 87 percent / NaH / dimethylsulfoxide
5: HCl / diethyl ether
6: dimethyl azodicarboxylate
With hydrogenchloride; potassium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; dichlorotriphenyl-λ4-phosphane; sodium hydride; diisobutylaluminium hydride; dimethyl azodicarboxylate; In diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/ja963113k
Guidance literature:
Multi-step reaction with 3 steps
1: 87 percent / NaH / dimethylsulfoxide
2: HCl / diethyl ether
3: dimethyl azodicarboxylate
With hydrogenchloride; sodium hydride; dimethyl azodicarboxylate; In diethyl ether; dimethyl sulfoxide;
DOI:10.1021/ja963113k
Guidance literature:
Multi-step reaction with 4 steps
1: 78 percent / Ph3PCl2 / CH2Cl2
2: 87 percent / NaH / dimethylsulfoxide
3: HCl / diethyl ether
4: dimethyl azodicarboxylate
With hydrogenchloride; dichlorotriphenyl-λ4-phosphane; sodium hydride; dimethyl azodicarboxylate; In diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/ja963113k
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