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3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide

Base Information Edit
  • Chemical Name:3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide
  • CAS No.:1446499-66-6
  • Molecular Formula:C23H32N2O4Si
  • Molecular Weight:428.604
  • Hs Code.:
  • Mol file:1446499-66-6.mol
3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide

Synonyms:3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide Edit
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Technology Process of 3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide

There total 10 articles about 3-(2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(phenyl)amino)-2-oxoethyl)-N-hydroxybenzamide 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 potassium cyanide; hydroxylamine; In tetrahydrofuran; methanol; at 20 ℃; for 16h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 7 steps
1.1: sulfuric acid / 5 h / Dean-Stark; Reflux
2.1: N,N-dimethyl-formamide / 18 h / Reflux
3.1: sodium hydroxide / methanol / 16 h / 90 °C
3.2: pH Ca.3
4.1: sulfuric acid / 18 h / Dean-Stark; Reflux
5.1: potassium carbonate / water; methanol / 12 h / 20 °C
6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h / 20 °C
7.1: hydroxylamine; potassium cyanide / tetrahydrofuran; methanol / 16 h / 20 °C / Inert atmosphere
With potassium cyanide; sulfuric acid; hydroxylamine; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1.1: N,N-dimethyl-formamide / 18 h / Reflux
2.1: sodium hydroxide / methanol / 16 h / 90 °C
2.2: pH Ca.3
3.1: sulfuric acid / 18 h / Dean-Stark; Reflux
4.1: potassium carbonate / water; methanol / 12 h / 20 °C
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h / 20 °C
6.1: hydroxylamine; potassium cyanide / tetrahydrofuran; methanol / 16 h / 20 °C / Inert atmosphere
With potassium cyanide; sulfuric acid; hydroxylamine; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
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