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6640-19-3

2-PHENOXYPROPIOPHENONE synthesis

9synthesis methods
-

Yield:6640-19-3 85%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide at 20; for 24 h;Inert atmosphere;Williamson Ether Synthesis;

Steps:

Synthesis of α-oxyketones 1d-p, 1s-w and 6

General procedure: General experimental procedure B (GEP-B): To a clean and oven-dried flask 1 equiv of the corresponding α-bromo ketone SM2-6 or desyl chloride (SM1), anhydrous DMF, 1.1-1.3 equiv of K2CO3 and 1.1-1.3 equiv of the corresponding phenol were added under nitrogen atmosphere. The mixture was allowed to react for 24 h at r.t. The reaction was worked up with H2O (15 mL) and extracted with Et2O (3 × 15 mL). The organic layers were combined, washed with aqueous NaOH (2 × 20 ml, 10% w/w) and dried over anhydrous Na2SO4. After evaporation under reduced pressure, the crude residue was purified by flash column chromatography on silica gel (eluent: hexane/EtOAc) to obtain α-oxy ketones 1 and 6.

References:

Sedano, Carlos;Virumbrales, Cintia;Suárez-Pantiga, Samuel;Sanz, Roberto [Synthesis,2021,vol. 53,# 20,p. 3725 - 3734] Location in patent:supporting information