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3506-70-5

4-(3-bromophenyl)butan-2-one synthesis

5synthesis methods
-

Yield:3506-70-5 94%

Reaction Conditions:

in tetrahydrofuran at -78 - 0;

Steps:

17

A solution of 3-(3-bromophenyl)-N-methoxy-N-methylpropanamide (Scheme 7, A)(0.500g, 1.84 mmol) and THF (18.0 mL) was cooled to -78° followed by the addition of 3.0 M methylmagnesium bromide (0.623 mL, 1.84 mmol) and allowed to stir at 00C for 2 h. Due to the presence of unreacted starting material, 3.0M methylmagnesium bromide (1.24 mL, 3.68 mmol) was added and allowed to stir overnight at O0C. The reaction was quenched with NH4Cl and the product extracted into DCM, dried ( Na2SO4) and concentrated to give product as a light orange liquid (0.391 g, 94%). 1H NMR (300 MHz, DMSO) δ 7.43 (s, IH)5 7.38 - 7.35 (m5 IH)5 7.25 - 7.21 (m, 2H)5 2.77 (s, 4H)5 2.09 (s, 3H),.m/z (APCI) M (226.9).

References:

WO2007/58601,2007,A1 Location in patent:Page/Page column 80

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