2-Bromopyridine → alpha-(4-Fluorophenyl)-alpha-(2-pyridyl)-4-piperidinemethanol

関与物質

反応条件

反応手順

To a stirred solution of 36.3 g (0.23 mol) of 2-bromopyridine in 500 mL of anhydrous tetrahydrofuran (THF) at -65° C. was added 88 mL (0.22 mol) of a commercial solution of 2.5M n-butyllithium in hexane at such a rate that the temperature did not exceed -60° C. The dark solution was stirred at -65° C. for 1 hr and then treated dropwise with a solution of 24.9 g (0.1 mol) of 1-acetyl-4-(p-fluorobenzoyl)piperidine (See Preparation 1 of U.S. Pat. No. 4,151,285, col. 4, lines 10-30, herein incorporated by reference) in 250 mL of THF at such a rate that the temperature did not exceed -60° C. The mixture was stirred for 1 hr at -65° C. and overnight at ambient temperature. The dark mixture was poured into 2 liters of a saturated ammonium chloride solution. The layers were separated and the aqueous layer was extracted once with a 500-mL portion of methylene chloride. The combined organic layers were washed successively with 500 mL of water, 500 mL of a 4% sodium hydroxide solution, 250 mL of water, and 250 mL brine.

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