2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

Base Information

Chemical Name:2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile
CAS No.:101836-08-2
Molecular Formula:C₂₁H₂₄N₂O₄
Molecular Weight:368.433
Hs Code.:

Synonyms:2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

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Chemical Property of 2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

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Technology Process of 2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

There total 4 articles about 2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-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: 48.0%

: 101836-05-9
2-<3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy>-6-nitrobenzonitrile

: 101836-08-2
2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

Guidance literature:: With hydrogen; cyclohexene; palladium on activated charcoal; In ethanol; for 0.5h; Heating;
DOI:10.1021/jm00157a004

Reference yield:

: 40786-20-7
4-<(3-bromopropyl)oxy>-2-hydroxy-3-propylacetophenone

: 101836-08-2
2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃, KI / acetone / 19 h / Heating

2: 48 percent / H₂, cyclohexene / 10percent Pd/C / ethanol / 0.5 h / Heating

With hydrogen; potassium carbonate; potassium iodide; cyclohexene; palladium on activated charcoal; In ethanol; acetone;
DOI:10.1021/jm00157a004

Reference yield:

: 38469-85-1
2-methoxy-6-nitrobenzonitrile

: 101836-08-2
2-amino-6-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-benzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / pyridine hydrochloride / 0.33 h / 200 °C

2: K₂CO₃, KI / acetone / 19 h / Heating

3: 48 percent / H₂, cyclohexene / 10percent Pd/C / ethanol / 0.5 h / Heating

With hydrogen; pyridine hydrochloride; potassium carbonate; potassium iodide; cyclohexene; palladium on activated charcoal; In ethanol; acetone;
DOI:10.1021/jm00157a004