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1-(5-bromopyridin-3-yl)ethanol synthesis

2synthesis methods
-

Yield:283608-66-2 98.1%

Reaction Conditions:

in tetrahydrofuran at 20; for 1 h;

Steps:

3.1 Step 1:

5-Bromonicotinic aldehyde (980mg, 5.0mmol), dissolved in 45mL THF, 1M methylmagnesium bromide solution (10mL, 10mmol) was added to the reaction at room temperature for 1 hour, 50mL saturated ammonium chloride was added to the reaction solution The aqueous solution was extracted with dichloromethane (100 mL×2), the organic phases were combined, washed with brine (100 mL×2), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure.Get 1-(5-bromopyridin-3-yl)ethanol(1.1 g, colorless liquid), yield: 98.1%

References:

CN111808086,2020,A Location in patent:Paragraph 0132-0134