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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | 3-(Diethylamino)-1-propanol | HCID 12159 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-diethyl-3-(4-nitrophenoxy)propan-1-amine | HCID 2057886 | 71.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098236B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-b8a7013060c64ea0a72ae1347253d224 |
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| Source note | uspto-grants-2006_08 |
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