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4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide

Base Information
  • Chemical Name:4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide
  • CAS No.:1443004-08-7
  • Molecular Formula:C22H34N2O4
  • Molecular Weight:390.523
  • Hs Code.:
4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide

Synonyms:4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide

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Chemical Property of 4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide
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Technology Process of 4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide

There total 5 articles about 4-cyano-N-methoxy-N-methyl-3,5-dihexyloxybenzamide 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:
4-cyano-3,5-dihexyloxybenzoic acid; isobutyl chloroformate; With 4-methyl-morpholine; In dichloromethane; at 0 ℃; for 0.333333h;
With hydroxylamine hydrochloride; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1039/c3ob40452h
Guidance literature:
Multi-step reaction with 3 steps
1.1: N,N-dimethyl-formamide / 48 h / 150 - 160 °C
2.1: tetrabutylammomium bromide; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 18 h
3.1: 4-methyl-morpholine / dichloromethane / 0.33 h / 0 °C
3.2: 1 h / 0 °C
With 4-methyl-morpholine; lithium hydroxide monohydrate; tetrabutylammomium bromide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c3ob40452h
Guidance literature:
Multi-step reaction with 5 steps
1.1: sulfuric acid / 18 h / Reflux
2.1: tetrabutylammomium bromide; potassium carbonate / acetone / 18 h / Reflux
3.1: N,N-dimethyl-formamide / 48 h / 150 - 160 °C
4.1: tetrabutylammomium bromide; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 18 h
5.1: 4-methyl-morpholine / dichloromethane / 0.33 h / 0 °C
5.2: 1 h / 0 °C
With 4-methyl-morpholine; lithium hydroxide monohydrate; sulfuric acid; tetrabutylammomium bromide; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; 2.1: |Williamson Ether Synthesis;
DOI:10.1039/c3ob40452h
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