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4-Methyl-N-(4-nitrophenyl)benzaMide synthesis

13synthesis methods
-

Yield:33667-88-8 92%

Reaction Conditions:

in neat (no solvent); for 0.0583333 h;Microwave irradiation;Green chemistry;

Steps:

General procedure for the synthesis of N-(aryl)- substituted benzamides [IIIa to IIIt]

General procedure: The reactants aniline, 250mg (2 mmol) and acid chloride, 250 mg (2 mmol) were thoroughly mixed in a crucible and exposure to microwave irradiation under solvent-free conditions using modified domestic microwave at 495 W for 3.5 min (Table I). The reaction course was carefully monitored by thin layer chromatogram (TLC) to regulate the reactant ratio, irradiation time, and microwave power level to achieve the maximum yield. The crude product (a powder), N-aryl- substituted benzamides thus obtained was washed with water and purified by recrystallization using 95% alcohol and dried under vacuum (Table I).

References:

Rao, Sri Latha;Veerabhadraswamy;Molkere, Bhimashankar B. [Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry,2020,vol. 59,# 6,p. 850 - 855]