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ChemicalBook CAS DataBase List 2-Chloro-5-acetylpyridine
55676-22-7

2-Chloro-5-acetylpyridine synthesis

11synthesis methods
53939-30-3 Synthesis
5-Bromo-2-chloropyridine

53939-30-3
460 suppliers
$5.00/1g

78191-00-1 Synthesis
N-Methoxy-N-methylacetamide

78191-00-1
280 suppliers
$6.00/5g

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Yield:55676-22-7 84%

Reaction Conditions:

Stage #1: 5-bromo-2-chloropyridinewith TurboGrignard in tetrahydrofuran at 0; for 0.25 h;Inert atmosphere;
Stage #2: N-Methoxy-N-methylacetamide in tetrahydrofuran at 0 - 20;Inert atmosphere;

Steps:

IM15: 1-(6-Chloro-pyridin-3-yl)-ethanone

A round bottomed flask was charged with 5-bromo-2-chloropyridine (5.30 g, 27.6 mmol) in THF under N2 and cooled at 0° C. A solution of 1 M iso-propylmagnesiumchloride-lithium chloride complex in THF (40 mL) was added drop wise over 15 min. After 70 min N-methoxy-N-methylacetamide (4.1 mL, 38 mmol) was added drop wise. After stirring for 5 min at 0° C. the cooling bath was removed. The mixture was left stirring overnight and was then quenched by the addition of 100 mL saturated aqueous NH4Cl solution. The mixture was extracted with 3×100 mL EtOAc. The combined organic layers were washed with water followed by brine and dried over MgSO4. Evaporation of the volatiles at 80° C., 10 mbar for 1 h gave the title compound (3.596 g, 84) sufficiently pure for the next step.

References:

US2013/12530,2013,A1 Location in patent:Paragraph 0187

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