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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11506Generated: October 26, 2026

p-Fluoronitrobenzene → N,N-diethyl-3-(4-nitrophenoxy)propan-1-amine

https://huagongshe.com/reaction/11506

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
Reactant3-(Diethylamino)-1-propanolHCID 12159—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diethyl-3-(4-nitrophenoxy)propan-1-amineHCID 205788671.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-diethylamino-1-propanol (2.97 mL, 20 mmol) in THF (40 mL) at 0° C. is treated potassium tert-butoxide (2.36 g, 1.05 equiv.) in one portion. The reaction mixture is stirred at 0° C. for 5 min during which time it becomes reddish brown. Neat 1-fluoro-4-nitrobenzene (2.82 g, 1 equiv.) is added dropwise and the ice-bath is removed. The reaction mixture is stirred at room temperature for 15 min. The dark green reaction mixture is quenched with ice-water (300 mL), and extracted with EtOAc (2×200 mL). The combined organic extracts are washed with water (2×300 mL) and brine (1×300 mL) and dried over anhydrous Na2SO4. The oily brown residue obtained after evaporation, is purified by chromatography, (silica gel, 1:4 MeOH:CHCl3) to give the named compound as a brown oil (3.59 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098236B2
Source datasetuspto-grants-2006_08
ORD IDord-b8a7013060c64ea0a72ae1347253d224
Source noteuspto-grants-2006_08