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ChemicalBook CAS DataBase List Valerophenone
1009-14-9

Valerophenone synthesis

12synthesis methods
Valerophenone is prepared from benzene and valeryl chloride by friedel-crafts reaction or from methyl benzoate by the Grignard reaction.
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Yield:1009-14-9 94%

Reaction Conditions:

with [2,2]bipyridinyl;palladium diacetate;trifluoroacetic acid in tetrahydrofuran;water at 80; for 36 h;Schlenk technique;Inert atmosphere;

Steps:

Alkyl Aryl Ketones 3 and 2-Arylbenzofurans 4; General Procedure

General procedure: To a Schlenk tube with a magnetic stirring bar were charged the respective nitrile 1 (0.4 mmol), arylboronic acid 2 (0.8 mmol), Pd(OAc)2 (5 mol%), bpy (10 mol%), TFA (10 equiv), THF (2 mL), and H2O (0.4 mL) under N2 atmosphere. The reaction mixture was stirred at 80 °C for 36 h. After cooling to r.t., the mixture was poured into EtOAc (5 mL), which was washed with sat. aq NaHCO3 (2*10 mL) and then brine (1*10 mL). After extracting the aqueous layer with EtOAc (3*10 mL), the combined organic layers were dried (Na2SO4), and evaporated under vacuum. The residue was purified by flash column chromatography (hexane-EtOAc) to afford the desired products 3 or 4. All known compounds afforded analytical data identical to those reported literature previously (see Supporting Information for further details).

References:

Wang, Xingyong;Wang, Xiaodong;Liu, Miaochang;Ding, Jinchang;Chen, Jiuxi;Wu, Huayue [Synthesis,2013,vol. 45,# 16,art. no. SS-2013-F0255-OP,p. 2241 - 2244]

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