ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

Base Information

Chemical Name:ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate
CAS No.:197707-94-1
Molecular Formula:C₃₁H₄₀O₇
Molecular Weight:524.654
Hs Code.:

Synonyms:ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

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Chemical Property of ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

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Technology Process of ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

There total 12 articles about ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate 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:

: 502-44-3,24980-41-4,80137-66-2
hexahydro-2H-oxepin-2-one

: 197707-94-1
ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

Guidance literature:: Multi-step reaction with 7 steps

1: conc. sulfuric acid / 1 h / Heating

2: AlCl₃ / 1,2-dichloro-ethane / 2.5 h / 15 °C

3: 5N aq. NaOH / methanol / 1 h / 25 °C

4: NaBH₄ / methanol / 1 h / 25 - 65 °C

5: 73 percent / KCl / dimethylsulfoxide / 4 h / 170 °C

6: 92 percent / triethylamine / CH₂Cl₂ / 1 h

7: 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 hydroxide; sodium tetrahydroborate; aluminium trichloride; sulfuric acid; potassium chloride; sodium hydride; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane;
DOI:10.1016/S0968-0896(97)00089-8

Reference yield:

: 128577-60-6
(5E)-6-(4-Methoxyphenyl)-5-hexen-1-ol

: 197707-94-1
ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / 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:

: 17814-85-6
(4-carboxybutyl)triphenylphosphonium bromide

: 197707-94-1
ethyl-4-{3-[2-(ethoxycarbonyl)ethyl]-4-[6-(4-methoxyphenyl)-(5E)-hexenyloxy]phenylcarbonyl}butanoate

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) t-BuOK / 1.) toluene, reflux, 30 min, 2.) toluene, 100 deg C, 10 min

2: conc. sulfuric acid / 1 h / 80 °C

3: 68 percent / LiAlH₄ / tetrahydrofuran / 0.5 h / 25 °C

4: 92 percent / triethylamine / CH₂Cl₂ / 1 h

5: 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; potassium tert-butylate; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0968-0896(97)00089-8