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99585-94-1

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

2synthesis methods
-

Yield:99585-94-1 97%

Reaction Conditions:

with triethylamine in ethyl acetate at 0 - 20; for 2 h;Inert atmosphere;

Steps:

General Procedure II

General procedure: To aniline (1.0 eq.) in ethyl acetate, 2-chloroacetyl chloride (1.1 eq.) was added. The reaction was then cooled to 0C and under N2. Triethylamine (1.1 eq.) was added dropwise, and the reaction was warmed to room temperature and stirred for 2 hours. The solvent was removed in vacuo and taken back up into ethyl acetate and water. Product,10, was purified by flash chromatography 0-40% EtOAc:hexanes.

References:

Tolentino, Kirsten T.;Mashinson, Viktoriya;Vadukoot, Anish K.;Hopkins, Corey R. [Bioorganic and Medicinal Chemistry Letters,2022,vol. 61,art. no. 128615] Location in patent:supporting information

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