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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816359Generated: October 31, 2026

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

https://huagongshe.com/reaction/1816359

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 numberUS06884803B2
Source datasetuspto-grants-2005_04
ORD IDord-76f6794fd1874c53a2bc6884bb9ff8c0
Source noteuspto-grants-2005_04