(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

Base Information

Chemical Name:(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene
CAS No.:950505-64-3
Molecular Formula:C₁₉H₂₀Br₂O₃
Molecular Weight:456.174
Hs Code.:

Synonyms:(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

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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 (E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

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Technology Process of (E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

There total 4 articles about (E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)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: 83.0%

: 950505-62-1
(5-(4-methoxybenzyloxy)-2-bromophenyl)methanol

: 821-06-7
(E)-1,4-dibromobutene

: 950505-64-3
(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

Guidance literature:: With sodium hydroxide; tetra-(n-butyl)ammonium iodide; In dichloromethane; water; at 20 ℃; for 17h;

Reference yield:

: 2973-80-0
2-bromo-5-hydroxybenzaldehyde

: 950505-64-3
(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 25 h / 20 °C

2: sodium tetrahydroborate / methanol / 4 h / Heating / reflux

3: sodium hydroxide; tetra-(n-butyl)ammonium iodide / dichloromethane; water / 17 h / 20 °C

With sodium hydroxide; sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; In methanol; dichloromethane; water;

Reference yield:

: 950505-60-9
5-(4-methoxybenzyloxy)-2-bromobenzaldehyde

: 950505-64-3
(E)-4-(4-methoxybenzyloxy)-1-bromo-2-((4-bromobut-2-enyloxy)methyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol / 4 h / Heating / reflux

2: sodium hydroxide; tetra-(n-butyl)ammonium iodide / dichloromethane; water / 17 h / 20 °C

With sodium hydroxide; sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; In methanol; dichloromethane; water;