3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

Base Information

Chemical Name:3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile
CAS No.:1228695-06-4
Molecular Formula:C₁₈H₁₃ClF₃N₃O₃
Molecular Weight:411.768
Hs Code.:

Synonyms:3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

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Chemical Property of 3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

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Technology Process of 3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

There total 5 articles about 3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile 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:

: 773837-37-9
sodium cyanide

: 1228695-05-3
4-(2-chloro-4-trifluoromethoxy-phenoxy)-3-(2-oxo-propoxy)-benzonitrile

: 1228695-06-4
3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

Guidance literature:: With ammonia; ammonium chloride; In ethanol; water; at 20 ℃; for 16h;

Reference yield:

: 243128-37-2
4-fluoro-3-methoxybenzonitrile

: 1228695-06-4
3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 120 °C

2.1: boron tribromide / dichloromethane / 20.5 h / 10 - 20 °C

2.2: Cooling with ice

3.1: potassium carbonate; potassium iodide / acetone / 4 h / Reflux

4.1: ammonia; ammonium chloride / ethanol; water / 16 h / 20 °C

With ammonia; boron tribromide; potassium carbonate; ammonium chloride; caesium carbonate; potassium iodide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;

Reference yield:

: 70783-75-4
4-(trifluoromethoxy)-2-chlorophenol

: 1228695-06-4
3-(2-amino-2-cyano-2-methyl-ethoxy)-4-(2-chloro-4-trifluoromethoxy-phenoxy)-benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 120 °C

2.1: boron tribromide / dichloromethane / 20.5 h / 10 - 20 °C

2.2: Cooling with ice

3.1: potassium carbonate; potassium iodide / acetone / 4 h / Reflux

4.1: ammonia; ammonium chloride / ethanol; water / 16 h / 20 °C

With ammonia; boron tribromide; potassium carbonate; ammonium chloride; caesium carbonate; potassium iodide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;