HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858184Generated: November 3, 2026
4-Nitrophenol → Diethyl[2-(4-nitrophenoxy)ethyl]amine
https://huagongshe.com/reaction/1858184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Chloro-2-(diethylamine)ethane hydrochloride | HCID 13363 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl[2-(4-nitrophenoxy)ethyl]amine | HCID 88294 | 66% |
Reaction Steps
A solution of 27.8 g (0.2 mol) of 4-nitrophenol in 500 ml of ethanol was treated with 15 g (0.22 mol) of sodium ethoxide. After stirring at room temperature for 30 minutes the solvent was removed under reduced pressure. The residual yellow solid was stirred in a mixture of 160 ml of xylene and 30 ml of water and then treated with 41.4 g (0.3 mol) of potassium carbonate and 34.4 g (0.2 mol) of 2-diethylaminoethyl chloride hydrochloride. The mixture was heated under reflux for 17 hours and filtered while hot. The filter residue was washed with hot xylene and the combined filtrate and washings were evaporated under reduced pressure. Distillation of the residue under a high vacuum gave 31.4 g (66%) of 4-[2-(diethylamino)ethoxy]-nitrobenzene as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150373 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-a53ac69b22754b48ab572b63f98ef2e5 |
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| Source note | uspto-grants-2000_11 |
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