5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

Base Information

Chemical Name:5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester
CAS No.:1396008-27-7
Molecular Formula:C₁₇H₁₄BrN₃O₂
Molecular Weight:372.221
Hs Code.:

Synonyms:5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

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Chemical Property of 5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

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Technology Process of 5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

There total 5 articles about 5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester 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: 99.0%

: 1396008-10-8
5-(4-bromo-phenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid

: 100-39-0
benzyl bromide

: 1396008-27-7
5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

Guidance literature:: With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 20 ℃; for 15h; Inert atmosphere;

Reference yield:

: 766-96-1
4-bromo-1-ethynylbenzene

: 1396008-27-7
5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -70 °C

1.2: 2 h / -70 - 20 °C

2.1: benzene / 4 h / Reflux

3.1: tetrabutyl ammonium fluoride; water / tetrahydrofuran / 0.17 h / 0 °C

4.1: water; lithium hydroxide / tetrahydrofuran / 3 h / 20 °C

5.1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 15 h / 20 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; water; sodium hydrogencarbonate; lithium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;

Reference yield:

: (4-bromo-phenyl)propynoic acid ethyl ester

: 1396008-27-7
5-(4-bromophenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: benzene / 4 h / Reflux

2: tetrabutyl ammonium fluoride; water / tetrahydrofuran / 0.17 h / 0 °C

3: water; lithium hydroxide / tetrahydrofuran / 3 h / 20 °C

4: sodium hydrogencarbonate / N,N-dimethyl-formamide / 15 h / 20 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; water; sodium hydrogencarbonate; lithium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;