Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827149Generated: October 30, 2026

1-Benzyl-4-hydroxypiperidine-4-carbonitrile → 4-(Aminomethyl)-1-benzylpiperidin-4-ol

https://huagongshe.com/reaction/1827149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-hydroxypiperidine-4-carbonitrileHCID 80189—
ReactantBorane;tetrahydrofuranHCID 2723981—
Product4-(Aminomethyl)-1-benzylpiperidin-4-olHCID 10421026—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-benzyl-4-hydroxy-piperidine-4-carbonitrile (5.00 g, 19.78 mmol) and BH3.THF (59.35 mmol, 59.35 mL, 1M in THF) was heated at 80° C. for 1 h. Cooled to 0° C. and quenched with conc. HCl (20 mL), the reaction solution was then stirred at rt in 1 h. The reaction solution was basified with 10N NaOH to pH8, and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water (50 mL), brine (30 mL), dried over Na2SO4, filtered and concentrated in vacuo to give 4-aminomethyl-1-benzyl-piperidin-4-ol. M.S.(M+1):221.31

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-285d5f9b9e8f4c6282a8ebac4808dbbb
Source noteuspto-grants-2006_05