(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

Base Information

Chemical Name:(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid
CAS No.:1450604-66-6
Molecular Formula:C₂₅H₂₁NO₄
Molecular Weight:399.446
Hs Code.:

Synonyms:(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

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Chemical Property of (αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

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Technology Process of (αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

There total 3 articles about (αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid 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: 71.0%

: 1450604-55-3
(αE)-α-[[1-acetyl-5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

: 1450604-66-6
(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; ethanol; at 70 ℃; for 2h;
DOI:10.1016/j.bmc.2013.06.030

Reference yield:

: 6953-22-6
5-benzyloxyindole-3-carboxaldehyde

: 1450604-66-6
(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic anhydride; triethylamine / 6 h / 130 °C

1.2: 16 h / 22 - 90 °C

2.1: sodium hydroxide / ethanol; tetrahydrofuran / 2 h / 70 °C

With acetic anhydride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmc.2013.06.030

Reference yield:

: 104-01-8
4-Methoxyphenylacetic acid

: 1450604-66-6
(αE)-α-[[5-(phenylmethoxy)-1H-indol-3-yl]methylene]-4-methoxybenzeneacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic anhydride; triethylamine / 6 h / 130 °C

1.2: 16 h / 22 - 90 °C

2.1: sodium hydroxide / ethanol; tetrahydrofuran / 2 h / 70 °C

With acetic anhydride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmc.2013.06.030