1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

Base Information

Chemical Name:1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide
CAS No.:1335568-36-9
Molecular Formula:Br*C₂₁H₁₈F₂N₃O
Molecular Weight:446.294
Hs Code.:

Synonyms:1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

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Chemical Property of 1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

Chemical Property:

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Technology Process of 1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

There total 3 articles about 1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium 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: 81.3%

: 13247-80-8
2-(2-bromoethoxy)naphthalene

: 1176849-82-3
1-(2,4-difluorobenzyl)-1H-1,2,4-triazole

: 1335568-36-9
1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

Guidance literature:: In acetonitrile; at 80 ℃;
DOI:10.1016/j.ejmech.2011.07.010

Reference yield:

: 135-19-3
β-naphthol

: 1335568-36-9
1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

Guidance literature:: Multi-step reaction with 2 steps

1: tetra-(n-butyl)ammonium iodide / 8 h / 78 °C

2: acetonitrile / 80 °C

With tetra-(n-butyl)ammonium iodide; In acetonitrile;
DOI:10.1016/j.ejmech.2011.07.010

Reference yield:

: 23915-07-3
1-(bromomethyl)-2,4-difluorobenzene

: 1335568-36-9
1-(2,4-difluorobenzyl)-4-(2-(naphthalen-2-yloxy)ethyl)-1H-1,2,4-triazol-4-ium bromide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / acetonitrile / 1 h / 60 °C

1.2: 45 °C

2.1: acetonitrile / 80 °C

With potassium carbonate; In acetonitrile;
DOI:10.1016/j.ejmech.2011.07.010