Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

Base Information

Chemical Name:Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide
CAS No.:73000-49-4
Molecular Formula:Br*C₂₆H₃₉N₂O
Molecular Weight:475.512
Hs Code.:

Synonyms:Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

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Chemical Property of Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

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Technology Process of Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

There total 4 articles about Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide 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:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 73000-49-4
Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / NaOEt / ethanol / 4 h / Heating

2: 74 percent / ethanol; H₂O / 38 h / 100 °C / sealed ampule

3: acetic acid / ethanol / 0.5 h / Heating

With sodium ethanolate; acetic acid; In ethanol; water;
DOI:10.1021/ja00522a019

Reference yield:

: 143773-73-3
4-(10-bromo-n-decyloxy)benzaldehyde

: 73000-49-4
Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / ethanol; H₂O / 38 h / 100 °C / sealed ampule

2: acetic acid / ethanol / 0.5 h / Heating

With acetic acid; In ethanol; water;
DOI:10.1021/ja00522a019

Reference yield:

: 4101-68-2
1,10-dibromodecane

: 73000-49-4
Trimethyl-(10-{4-[(E)-phenyliminomethyl]-phenoxy}-decyl)-ammonium; bromide

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / NaOEt / ethanol / 4 h / Heating

2: 74 percent / ethanol; H₂O / 38 h / 100 °C / sealed ampule

3: acetic acid / ethanol / 0.5 h / Heating

With sodium ethanolate; acetic acid; In ethanol; water;
DOI:10.1021/ja00522a019