[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

Base Information

Chemical Name:[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester
CAS No.:251943-44-9
Molecular Formula:C₂₇H₂₉N₄O₃P
Molecular Weight:488.526
Hs Code.:

[1-(benzhydrylidene-amino)-2-(1-phenyl-1<i>H</i>-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

Synonyms:[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

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Chemical Property of [1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

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Technology Process of [1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

There total 3 articles about [1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl 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: 68.0%

: 127780-58-9
diethyl α-propargyl-N-(diphenylmethylene)aminomethylphosphonate

: 622-37-7
Phenyl azide

: 251943-44-9
[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

Guidance literature:: In benzene; at 120 ℃; for 4h;

Reference yield:

: 1013-88-3
Benzophenone imine

: 251943-44-9
[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / CH₂Cl₂ / 24 h / 20 °C

2: 75 percent / KOH / 20 °C

3: 68 percent / benzene / 4 h / 120 °C

With potassium hydroxide; In dichloromethane; benzene; 1: Condensation / 2: Alkylation / 3: Cycloaddition;

Reference yield:

: 122570-91-6
diethyl N-(diphenylmethylene) aminomethyl phosphonate

: 251943-44-9
[1-(benzhydrylidene-amino)-2-(1-phenyl-1H-[1,2,3]triazol-4-yl)-ethyl]-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / KOH / 20 °C

2: 68 percent / benzene / 4 h / 120 °C

With potassium hydroxide; In benzene; 1: Alkylation / 2: Cycloaddition;