ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

Base Information

Chemical Name:ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate
CAS No.:1069049-10-0
Molecular Formula:C₂₉H₃₁NO₄
Molecular Weight:457.569
Hs Code.:

Synonyms:ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

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Technology Process of ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

There total 6 articles about ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}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: 43.0%

: 1069048-09-4
ethyl 3-[3-(2-phenylethyl)-1H-indol-5-yl]propanoate

: 34743-88-9
2-(4-bromophenoxy)ethanol

: 1069049-10-0
ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

Guidance literature:: With potassium phosphate; palladium diacetate; johnphos; In acetic acid butyl ester; at 110 - 120 ℃;
DOI:10.1021/jm500494y

Reference yield:

: 127876-36-2
2-(benzotriazol-1-yl)acetophenone

: 1069049-10-0
ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

Guidance literature:: Multi-step reaction with 5 steps

1: titanium tetrachloride / dichloromethane / 3 h / 20 °C

2: lithium aluminium tetrahydride / diethyl ether / 2.5 h / 20 °C

3: palladium diacetate; tris-(o-tolyl)phosphine; triethylamine / toluene / 110 °C

4: palladium on activated charcoal; hydrogen / ethanol / 20 °C

5: johnphos; potassium phosphate; palladium diacetate / acetic acid butyl ester / 110 - 120 °C

With potassium phosphate; lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; palladium diacetate; titanium tetrachloride; triethylamine; tris-(o-tolyl)phosphine; johnphos; In diethyl ether; ethanol; dichloromethane; acetic acid butyl ester; toluene; 3: |Heck Reaction;
DOI:10.1021/jm500494y

Reference yield:

: 1069051-39-3
1-(5-bromo-1H-indol-3-yl)-2-phenylethanone

: 1069049-10-0
ethyl 3-{1-[4-(2-hydroxyethoxy)phenyl]-3-(2-phenylethyl)-1H-indol-5-yl}propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminium tetrahydride / diethyl ether / 2.5 h / 20 °C

2: palladium diacetate; tris-(o-tolyl)phosphine; triethylamine / toluene / 110 °C

3: palladium on activated charcoal; hydrogen / ethanol / 20 °C

4: johnphos; potassium phosphate; palladium diacetate / acetic acid butyl ester / 110 - 120 °C

With potassium phosphate; lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; palladium diacetate; triethylamine; tris-(o-tolyl)phosphine; johnphos; In diethyl ether; ethanol; acetic acid butyl ester; toluene; 2: |Heck Reaction;
DOI:10.1021/jm500494y