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2-Pyridinamine, N-[(4-nitrophenyl)methylene]- synthesis

3synthesis methods
-

Yield:5918-77-4 85%

Reaction Conditions:

with acetic acid in methanol; for 3 h;Reflux;

Steps:

3.2. General Procedure for the Synthesis of Compounds 1-12

General procedure: An equal molar solution of a primary amine (0.01 mol) and an aldehyde (0.01 mol) in dry methanol(50 mL) was refluxed for 3 h using a few drops of acetic acid as a catalyst. The reaction mixture wasthen cooled to room temperature and the formed precipitate was filtered, washed with methanol 35 mL) and diethyl ether (2 5 mL), and then dried under vacuum. The recrystallization frommethanol/dioxane (1:4) mixture gave pure products (1-12).

References:

Toubi, Yahya;Abrigach, Farid;Radi, Smaail;Souna, Faiza;Hakkou, Abdelkader;Alsayari, Abdulrhman;Muhsinah, Abdullatif Bin;Mabkhot, Yahia N. [Molecules,2019,vol. 24,# 18,art. no. 3250]