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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455174Generated: October 31, 2026

Piperidine → 1-[(4-Bromophenyl)methyl]piperidine

https://huagongshe.com/reaction/1455174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product1-[(4-Bromophenyl)methyl]piperidineHCID 16495045—

Reaction Steps

A solution of 4-bromobenzaldehyde (5 g), piperidine (2.9 mL), and acetic acid (1.5 mL) in DCE (65 mL) was treated with sodium triacetoxyborohydride (6.9 g). After 27 h, the resulting mixture was treated with saturated aqueous sodium bicarbonate (50 mL), and extracted with DCM (2×50 mL). The combined organic phases were dried (magnesium sulfate) and evaporated. Kugelrohr distillation of the residue (160° C., 5 mm Hg) gave the title compound as a pale yellow oil (5.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482364B2
Source datasetuspto-grants-2009_01
ORD IDord-3d2f066ae78c4e5f9f73ff58cffaf0a5
Source noteuspto-grants-2009_01