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ChemicalBook CAS DataBase List 3-Fluoroacetanilide
351-28-0

3-Fluoroacetanilide synthesis

15synthesis methods
-

Yield: 83%

Reaction Conditions:

with 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate at 90; for 0.166667 h;Microwave irradiation;chemoselective reaction;Temperature;

Steps:

Typical procedure for N-acylation Amines (microwave irradiation):
General procedure: A mixture of amines (0.01 mol), acetic acid (0.015 mol, 1 mL) and [BMIM(SO3H)][OTf] (50 mol %) was introduced into a Biotage microwave oven and heated for 6 to 9 minutes at 90oC. Progress of the reaction was monitored by TLC and GC-MS. After completion of reaction, the reaction mass was cooled at room temperature and poured into ice water. The crystals of N-acylated product so obtained were filtered, washed with of cold ethanol-water mixture (10-15mL) and dried.

References:

Savanur, Hemantkumar M.;Malunavar, Shruti S.;Prabhala, Pavankumar;Sutar, Suraj M.;Kalkhambkar, Rajesh G.;Laali, Kenneth K. [Tetrahedron Letters,2019,vol. 60,# 42,art. no. 151159] Location in patent:supporting information

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