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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518765Generated: October 31, 2026

Piperidine → 1-(3-Fluoro-4-nitrobenzyl)piperidine

https://huagongshe.com/reaction/518765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
Reactant3-Fluoro-4-nitrobenzaldehydeHCID 3808120—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product1-(3-Fluoro-4-nitrobenzyl)piperidineHCID 6672851458.2%

Reaction Steps

To a mixture of 3-fluoro-4-nitrobenzaldehyde (4.85 g, 28.7 mmol), piperidine (3.12 mL, 31.5 mmol) and 20 drops of AcOH in DCM was added sodium triacetoxyborohydride (6.69 g, 31.5 mmol), and the resulting suspension was stirred at RT for 30 minutes. The reaction was made basic with 2N aqueous NaOH, and extracted with DCM. The organic layer was washed with brine and was dried over sodium sulfate, filtered and concentrated in vacuo to yield a red oil. The residual oil was purified via MPLC, eluting with a gradient of 0-100% EtOAc in hexane to yield 1-(3-fluoro-4-nitrobenzyl)piperidine (3.98 g, 16.70 mmol, 58.2% yield) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-309246382b44426bbb1cf008a67d8c61
Source noteuspto-grants-2015_08