ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

Base Information

Chemical Name:ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate
CAS No.:197707-77-0
Molecular Formula:C₃₃H₄₆N₂O₆
Molecular Weight:566.738
Hs Code.:

Synonyms:ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

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Chemical Property of ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

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Technology Process of ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

There total 4 articles about ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate 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:

: 197708-41-1
(E)-6-(4-Propoxy-phenyl)-hex-5-en-1-ol

: 197707-77-0
ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 1 h

2: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With sodium hydride; triethylamine; In dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8

Reference yield:

: 6-(p-propoxyphenyl)-5-hexenoic acid

: 197707-77-0
ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: conc. sulfuric acid / 1 h / 80 °C

2: LiAlH₄ / tetrahydrofuran / 0.5 h / 25 °C

3: triethylamine / CH₂Cl₂ / 1 h

4: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With lithium aluminium tetrahydride; sulfuric acid; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8

Reference yield:

: 197708-38-6
(E)-6-(4-Propoxy-phenyl)-hex-5-enoic acid ethyl ester

: 197707-77-0
ethyl-3-{2-[6-(4-n-propyloxyphenyl)-(5E)-hexenyloxy]-5-[4-(dimethylaminocarbonyl)butanoylamino]phenyl}propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: LiAlH₄ / tetrahydrofuran / 0.5 h / 25 °C

2: triethylamine / CH₂Cl₂ / 1 h

3: 1.) NaH / 1.) DMF, a) from 0 deg C to 25 deg C, b) 25 deg C, 30 min, 2.) DMF, 60 deg C, 2 h

With lithium aluminium tetrahydride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8