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20876-27-1

(2-Methoxy-6-nitrophenyl)acetonitrile synthesis

11synthesis methods
773837-37-9 Synthesis
sodium:cyanide

773837-37-9
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Yield: 61%

Reaction Conditions:

in ethanolReflux;

Steps:

84
Reference Example 84; (2-methoxy-6-nitro-phenyl)-acetonitrile; Sodium cyanide (165 mg, 3.36 mmol) was added to a solution of 2-bromomethyl-1-methoxy-3-nitro-benzene (680 mg, 2.56 mmol) in ethanol (5 mL) and the mixture was heated at reflux overnight. The solvent was removed in vacuo, water (30 mL) was added and the mixture was extracted with dichloromethane (25 mL). The organic phase was washed with water (2×20 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude compound was purified by column chromatography over silica gel (100-200 mesh) using 8% ethyl acetate in petroleum ether to afford (2-methoxy-6-nitro-phenyl)-acetonitrile (300 mg, 61%).

References:

F2G LIMITED US2011/9390, 2011, A1 Location in patent:Page/Page column 23