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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993519Generated: October 26, 2026

Piperidine → 1-(2-Methoxy-4-nitrophenyl)piperidine

https://huagongshe.com/reaction/1993519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-Bromo-5-nitroanisoleHCID 101293—
SolventWaterHCID 962—
Product1-(2-Methoxy-4-nitrophenyl)piperidineHCID 2825431—

Reaction Steps

2-Bromo-5-nitroanisole (5.0 g, 21.5 mmol) and piperidine (8.5 ml) is stirred for 5 h at 105° C. under N2-atmosphere. Water (80 ml) is added and the mixture is extracted twice with CH2Cl2 (2×80 ml). The organic phases are washed with water and brine, dried (Na2SO4) and concentrated. The crude product is dissolved in AcOEt, SiO2 is then added and the solvent evaporate off In vacuo. The resulting powder is put on top of a chromatography column (SiO2; AcOEt/hexane 9:1) and the title compound eluted with hexane/AcOEt 9:1→4:1: MS: [M+1]+=237; Rf=0.2 (AcOEt/hexane 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652022B2
Source datasetuspto-grants-2010_01
ORD IDord-3dd255ab30d143e89b68187a2849a7b5
Source noteuspto-grants-2010_01