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2-CHLORO-N-(3-CHLORO-4-METHYLPHENYL)ACETAMIDE synthesis

3synthesis methods
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Yield:99585-97-4 67%

Reaction Conditions:

with pyridine in benzene at 20 - 60; for 5 h;

Steps:

2-Haloacetamides 8a-8d and 9a-9d (general procedure)

General procedure: A solution of 0.02 mol of bromo- orchloroacetamide in 40 mL of dry benzene was addedto mixture of 0.02 mol of amine 6a, 6b, or 7a-7c and1.6 g (0.02 mol) of dry pyridine in 70 mL of dry benzeneunder stirring and cooling with ice water. The reactionmixture was stirred at room temperature for 4 h and then1 h at 60°C. After cooling, 30 mL of water was added,the layers were separated, the benzene layer was washedwith water, and the solvent was removed by distillation.The residue was crystallied and recrystallized.

References:

Arustamyan, Zh. S.;Margaryan;Aghekyan;Panosyan;Muradyan;Tumajyan [Russian Journal of Organic Chemistry,2021,vol. 57,# 2,p. 195 - 202][Zh. Org. Khim.,2021,vol. 57,# 2,p. 230 - 238,8]

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