HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17658Generated: October 25, 2026
3-Nitrophenol → N,N-diethyl-N-[3-(3-nitrophenoxy)propyl]amine
https://huagongshe.com/reaction/17658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | Diethylamino-propanol | HCID 5256659 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-diethyl-N-[3-(3-nitrophenoxy)propyl]amine | HCID 22012884 | — |
Reaction Steps
To a stirred solution of 3-nitrophenol (2 mmol) in DMF (6 mL) at rt, solid potassium carbonate (4 mmol) was added. A solution of the mesylate of N,N-diethylaminopropanol (2.2 mmol) in DMF (2 mL) was then added to the reaction mixture and heated to 80° C. until completion, according to General Procedure Q1, as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was then treated with cold H2O (15 mL), and extracted with EtOAc (2×15 mL). The combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of the solvent in vacuuo afforded the desired N,N-diethyl-N-[3-(3-nitrophenoxy)propyl]amine. The crude product was used directly for further transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737285B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1a59dbac1df94d85990d11a3d8f7174d |
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| Source note | uspto-grants-2010_06 |
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