tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

Base Information

Chemical Name:tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate
CAS No.:1448674-31-4
Molecular Formula:C₁₆H₂₃N₃O₄
Molecular Weight:321.376
Hs Code.:

Synonyms:tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

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Chemical Property of tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

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Technology Process of tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

There total 5 articles about tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate 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:

Reference yield: 55.0%

: 1448674-30-3
tert-butyl [2-(4-cyanophenoxy)ethoxy]carbamate

: 107-15-3,85404-18-8
ethylenediamine

: 1448674-31-4
tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

Guidance literature:: With sodium hydrogen sulfide; at 120 ℃; for 2h;

Reference yield:

: 37142-39-5
4-(2-bromoethoxy)benzonitrile

: 1448674-31-4
tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 6 h / 46 °C

2: hydrazine hydrate / ethanol / 14 h / 45 °C

3: triethylamine / dichloromethane / 20 °C

4: sodium hydrogen sulfide / 2 h / 120 °C

With sodium hydrogen sulfide; hydrazine hydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 767-00-0
4-cyanophenol

: 1448674-31-4
tert-butyl {2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]ethoxy}carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / acetonitrile / 18 h / Reflux

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 6 h / 46 °C

3: hydrazine hydrate / ethanol / 14 h / 45 °C

4: triethylamine / dichloromethane / 20 °C

5: sodium hydrogen sulfide / 2 h / 120 °C

With sodium hydrogen sulfide; potassium carbonate; hydrazine hydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;