HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1793462Erstellt: 25. Oktober 2026
P-Anisidine → (4-Methoxyphenyl)-(3-(naphthalen-2-yloxy)propyl)amine
https://huagongshe.com/reaction/1793462
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | P-Anisidine | HCID 7732 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(2-Naphthyloxy)-1-chloropropane | HCID 11687205 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (4-Methoxyphenyl)-(3-(naphthalen-2-yloxy)propyl)amine | HCID 9839556 | — |
Reaktionsschritte
A mixture of anhydrous potassium carbonate (10 gm, in excess) and p-anisidine (0.42 gm, 0.003 mole) was taken in dry DMF (40 ml). Now 3-(2-naphthyloxy)-1-chloropropane (0.5 gm, 0.002 mole) was added in it. Reaction mixture was refluxed at 140° C. for 7 hrs and the reaction was completed as checked by TLC. Reaction mixture was poured in distilled water (60 ml) and extracted with ethyl acetate thrice. The organic layer was separated and concentrated to get oily compound which was later crystallized by benzene hexane to get N-(4-methoxyphenyl)-[3-(naphthalen-2-yloxy) propyl]amine as yellow solid, m.p. 110° C., (yield 0.64 gm, 92.5%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07081465B2 |
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| Quelldatensatz | uspto-grants-2006_07 |
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| ORD ID | ord-0c6366e473ff4c269f7ad5920603d475 |
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| Quellennotiz | uspto-grants-2006_07 |
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