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(R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate

Base Information
  • Chemical Name:(R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate
  • CAS No.:1432740-77-6
  • Molecular Formula:C21H22ClN3O2
  • Molecular Weight:383.878
  • Hs Code.:
(R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate

Synonyms:

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Chemical Property of (R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate
Chemical Property:
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Technology Process of (R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate

There total 3 articles about (R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethyl 4-isopropylphenylcarbamate 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:
(R)-1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethanol; With sodium hydride; In acetonitrile; at 20 ℃; for 2h;
4-isopropylphenylisocyanate; at 20 ℃; for 24h;
DOI:10.1021/jm500739f
Guidance literature:
Multi-step reaction with 3 steps
1.1: N,N-dimethyl-formamide / 2 h / 0 °C
2.1: Noyori's catalyst; formic acid; triethylamine / dichloromethane / 26 h / 40 °C / Inert atmosphere
3.1: sodium hydride / acetonitrile / 2 h / 20 °C
3.2: 24 h / 20 °C
With Noyori's catalyst; formic acid; sodium hydride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm500739f
Guidance literature:
Multi-step reaction with 2 steps
1.1: Noyori's catalyst; formic acid; triethylamine / dichloromethane / 26 h / 40 °C / Inert atmosphere
2.1: sodium hydride / acetonitrile / 2 h / 20 °C
2.2: 24 h / 20 °C
With Noyori's catalyst; formic acid; sodium hydride; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm500739f
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