(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

Base Information

Chemical Name:(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)
CAS No.:1376231-79-6
Molecular Formula:C₃₆H₃₁Br₂N₃
Molecular Weight:665.47
Hs Code.:

Synonyms:(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

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Chemical Property of (2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

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Technology Process of (2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

There total 4 articles about (2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile) 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: 44.0%

: 16532-79-9
4-Bromophenylacetonitrile

: 207129-05-3
4,4'-(hexylazanediyl)dibenzaldehyde

: 1376231-79-6
(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

Guidance literature:: With potassium tert-butylate; In methanol; at 20 ℃;
DOI:10.1016/j.dyepig.2012.02.016

Reference yield:

: 111-25-1
1-bromo-hexane

: 1376231-79-6
(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / dimethyl sulfoxide / 110 °C

2.1: trichlorophosphate / 0 °C / Inert atmosphere

2.2: 95 °C / Inert atmosphere

3.1: potassium tert-butylate / methanol / 20 °C

With potassium tert-butylate; sodium hydroxide; trichlorophosphate; In methanol; dimethyl sulfoxide; 2.1: Vilsmeier formylation / 2.2: Vilsmeier formylation / 3.1: Knoevenagel condensation;
DOI:10.1016/j.dyepig.2012.02.016

Reference yield:

: N-hexyl-N-phenylbenzenamine

: 1376231-79-6
(2Z,2'Z)-3,3'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(2-(4-bromophenyl)acrylonitrile)

Guidance literature:: Multi-step reaction with 2 steps

1.1: trichlorophosphate / 0 °C / Inert atmosphere

1.2: 95 °C / Inert atmosphere

2.1: potassium tert-butylate / methanol / 20 °C

With potassium tert-butylate; trichlorophosphate; In methanol; 1.1: Vilsmeier formylation / 1.2: Vilsmeier formylation / 2.1: Knoevenagel condensation;
DOI:10.1016/j.dyepig.2012.02.016