N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

Base Information

Chemical Name:N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester
CAS No.:101835-99-8
Molecular Formula:C₂₆H₃₀N₂O₈
Molecular Weight:498.533
Hs Code.:

Synonyms:N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

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Chemical Property of N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

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Technology Process of N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

There total 5 articles about N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester 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: 14.0%

: 91324-97-9
2-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)-2-hydroxypropoxy]-6-aminobenzonitrile

: 36239-09-5
ethyl chlorocarbonylacetate

: 101835-99-8
N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

Guidance literature:: In dichloromethane; 1.) 0 deg C, 40 min, 2.) 25 deg C, 3 h;
DOI:10.1021/jm00157a004

Reference yield:

: 57161-85-0
3-(2-n-Propyl-3-hydroxy-4-acetylphenoxy)-1,2-epoxypropane

: 101835-99-8
N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Triton B / dimethylformamide / 1.5 h / Heating

2: 66 percent / cyclohexene / 10percent Pd/C / ethanol / 0.5 h / Heating

3: 14 percent / CH₂Cl₂ / 1.) 0 deg C, 40 min, 2.) 25 deg C, 3 h

With N-benzyl-trimethylammonium hydroxide; cyclohexene; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00157a004

Reference yield:

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

: 101835-99-8
N-{3-[3-(4-Acetyl-3-hydroxy-2-propyl-phenoxy)-2-hydroxy-propoxy]-2-cyano-phenyl}-malonamic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

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

2: Triton B / dimethylformamide / 1.5 h / Heating

3: 66 percent / cyclohexene / 10percent Pd/C / ethanol / 0.5 h / Heating

4: 14 percent / CH₂Cl₂ / 1.) 0 deg C, 40 min, 2.) 25 deg C, 3 h

With pyridine hydrochloride; N-benzyl-trimethylammonium hydroxide; cyclohexene; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00157a004