Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Ethylazetidin-3-ol | HCID 13813928 | — |
| Product | HCID 13055702 | HCID 13055702 | 70% |
Reaction Steps
To a mixture of 10.2 parts of 1-ethyl-3-azetidinol and 14.4 parts of α-naphthol 0.2 part of potassium hydroxide was added, and the mixture was heated under nitrogen gas at 160° C. for 18 hours. The reaction mixture was cooled and extracted with ether. The ether extract was washed with 2N-NaOH aqueous solution and then with water. The liquor was dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was recrystallized from cyclohexane to yield 17.2 parts of 1-(α-naphthoxy)-3-ethylamino-2-propanol. The melting of the product was 106°-107° C. The yield was 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018824 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-57e0804322d142c0a0c4f9d760ee75fd |
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| Source note | uspto-grants-1977_04 |
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