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1496-76-0

(1H-indol-1-yl)(phenyl)methanone synthesis

12synthesis methods
-

Yield:1496-76-0 99%

Reaction Conditions:

with sodium carbonate in acetonitrile at 120; for 24 h;Schlenk technique;regioselective reaction;

Steps:

Na2CO3-Catalyzed N-Acylation of Indoles; General Procedure

General procedure: A mixture of indole 1 (0.50 mmol), Na2CO3 (10.6 mg, 0.10 mmol, 20 mol%), and alkenyl carboxylate 2 (2.0 mmol, 4.0 equiv) in MeCN (3 mL) was added into a Schlenk flask (25 mL) and stirred at 120 °C until completion of the reaction. Then the solvent was evaporated under reduced pressure and the residue was purified by column chromatography (petroleum ether/EtOAc 20:1 to 5:1) to afford the desired acylindoles 3 (Tables 2 and 3).

References:

Zhou, Xiao-Yu;Chen, Xia [Synthesis,2019,vol. 51,# 2,p. 516 - 521] Location in patent:supporting information