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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640998Generated: October 29, 2026

1-Fluoro-2-nitrobenzene → 1-(4-Nitrophenyl)-4-piperidinol

https://huagongshe.com/reaction/640998

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantPiperidin-4-olHCID 79341—
ReactantDiisopropylethylamineHCID 81531—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Nitrophenyl)-4-piperidinolHCID 613768145.2%

Reaction Steps

A 100 mL round bottom flask was dried in an oven overnight and cooled to room temperature under Ar(g). The flask was charged with fluoronitrobenzene (0.500 mL, 4.71 mmol), Piperidin-4-ol (0.619 g, 2.30 mmol) and dioxane (9.0 mL). To the resulting solution, diisopropyl ethyl amine (0.463 mL, 6.12 mmol) was added dropwise, and the reaction was allowed to stir at 105° C. for 48 h. The mixture was extracted with EtOAc (3ט50 mL), and brine (2ט50 mL). The combined organic layers were then dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The crude mixture was then purified over silica (10% MeOH/90% CHCl3) affording a yellow solid (0.742 g, 3.34 mmol, 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692005B2
Source datasetuspto-grants-2010_04
ORD IDord-312e8b9d608149058b3b61491211c47e
Source noteuspto-grants-2010_04