HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328898Erstellt: 25. Oktober 2026
2-Naphthol → 1-(beta-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane
https://huagongshe.com/reaction/328898
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Naphthol | HCID 8663 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 1-(Iso-propyl)-3-benzyloxyazetidine | HCID 20517324 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-(beta-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane | HCID 13055713 | 84% |
Reaktionsschritte
A mixture of 17.3 parts of β-naphthol, 20.5 parts of 1-(iso-propyl)-3-benzyloxyazetidine, and 1.1 parts of potassium hydroxide was heated under nitrogen gas at 180° C. for 8 hours with agitation. The reaction mixture was cooled and dissolved in 100 parts of ether. The solution was washed with 50 parts of 2N-sodium hydroxide aqueous solution and dried over anhydrous sodium sulfate. Ether was distilled off and the residue was subjected to distillation to yield 29.3 parts of 1-(β-naphthoxy)-2-benzyloxy-3-(iso-propylamino)propane boiling at 185° -190° C. under 1 mm Hg. The yield was 84%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the product are as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04018824 |
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| Quelldatensatz | uspto-grants-1977_04 |
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| ORD ID | ord-2f48bb655e6745d28b97b9dbbda54b93 |
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| Quellennotiz | uspto-grants-1977_04 |
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