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887593-76-2

2-(4-HYDROXY-PIPERIDIN-1-YLMETHYL)-BENZONITRILE synthesis

1synthesis methods
22115-41-9 Synthesis
2-Cyanobenzyl bromide

22115-41-9
451 suppliers
$5.00/5g

2-(4-HYDROXY-PIPERIDIN-1-YLMETHYL)-BENZONITRILE

887593-76-2
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Yield:887593-76-2 86%

Reaction Conditions:

with pyridine in tetrahydrofuran; for 1 h;Product distribution / selectivity;Heating / reflux;

Steps:

10

To a solution of 4-hydroxypiperidine (1.00 g, 0.01 mmol) and α-bromotolunitrile (2.91 g, 0.015 mmol) in 20 mL THF was added pyridine (1.62 mL, 0.02 mmol). The reaction mixture was heated to reflux for 1 hour. Solvents were removed under reduced pressure and the crude product purified by column chromatography (CH2Cl2/MeOH: 95/5) to give 1.86 g (86%) of the desired compound.

References:

US2009/23773,2009,A1 Location in patent:Page/Page column 55-56