1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

Base Information

Chemical Name:1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene
CAS No.:1314093-93-0
Molecular Formula:C₂₉H₃₀F₃NO₆
Molecular Weight:545.556
Hs Code.:

Synonyms:1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

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Chemical Property of 1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

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Technology Process of 1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

There total 7 articles about 1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene 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: 96.0%

: 1314093-91-8
1,3-bis(4-methoxybenzyloxy)-6-(3-hydroxyprop-1-ynyl)-5-[2-(trifluoroacetamido)ethyl]benzene

: 1314093-93-0
1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

Guidance literature:: With sodium tetrahydroborate; N,N,N,N,-tetramethylethylenediamine; hydrogen; nickel diacetate; In ethanol; for 18h; under 760.051 Torr;
DOI:10.1021/jo2009615

Reference yield:

: 1314093-97-4
3,5-bis(4-methoxybenzyloxy)benzaldehyde

: 1314093-93-0
1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonium acetate / 1.5 h / Reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 65 °C

2.2: 1 h / 0 °C

3.1: N-iodo-succinimide / N,N-dimethyl-formamide / 18 h / 20 °C

4.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 0.33 h / 30 °C

4.2: 48 h / Reflux

5.1: sodium tetrahydroborate; N,N,N,N,-tetramethylethylenediamine; hydrogen; nickel diacetate / ethanol / 18 h / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; N-iodo-succinimide; copper(l) iodide; lithium aluminium tetrahydride; N,N,N,N,-tetramethylethylenediamine; ammonium acetate; hydrogen; nickel diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 4.1: Sonogashira coupling / 4.2: Sonogashira coupling;
DOI:10.1021/jo2009615

Reference yield:

: 1314093-99-6
1,3-bis(4-methoxybenzyloxy)-5-[(E)-2-nitroethenyl]benzene

: 1314093-93-0
1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 65 °C

1.2: 1 h / 0 °C

2.1: N-iodo-succinimide / N,N-dimethyl-formamide / 18 h / 20 °C

3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 0.33 h / 30 °C

3.2: 48 h / Reflux

4.1: sodium tetrahydroborate; N,N,N,N,-tetramethylethylenediamine; hydrogen; nickel diacetate / ethanol / 18 h / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; N-iodo-succinimide; copper(l) iodide; lithium aluminium tetrahydride; N,N,N,N,-tetramethylethylenediamine; hydrogen; nickel diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 3.1: Sonogashira coupling / 3.2: Sonogashira coupling;
DOI:10.1021/jo2009615