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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyl-4-hydroxypiperidine-4-carbonitrile | HCID 80189 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Product | 4-(Aminomethyl)-1-benzylpiperidin-4-ol | HCID 10421026 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053089B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-285d5f9b9e8f4c6282a8ebac4808dbbb |
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| Source note | uspto-grants-2006_05 |
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