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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30470Generated: October 26, 2026

Piperidine → 3-Bromo-5-(piperidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/30470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product3-Bromo-5-(piperidin-1-ylmethyl)pyridineHCID 6718880571%

Reaction Steps

5-Bromo-pyridine-3-carbaldehyde (0.190g, 1 mmol), NaB(OAc)3H (0.320 g, 1.50 mmol) and piperidine (0.090 g, 1.05 mmol) were suspended in DCM (8 mL) and the reaction mixture was stirred overnight at rt. The reaction was quenched by the addition of 1 M NaOH solution (5 mL) and the mixture was stirred for 1 h. The reaction mixture was extracted with DCM (3×15 mL). The organic extracts were combined, dried over Na2SO4, filtered, and concentrated to yield a crude oily product (0.18 g, 71%). This crude product was carried to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423147B2
Source datasetuspto-grants-2008_09
ORD IDord-f27ee76980884117baec2023d5ba8948
Source noteuspto-grants-2008_09