Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 2,3-Dimethylphenol | HCID 10687 | — |
| Edukt | 1-tert-Butyl-3-hydroxyazetidine | HCID 287986 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Xibenolol | HCID 146256 | — |
Reaktionsschritte
A mixture of 4.8 parts of 1-(tert.-butyl)-3-azetidinol, 6.1 parts of 2,3-xylenol and 1.4 parts of trifluoroacetic acid was heated at 130° C. for 12 hours. The reaction mixture was cooled and dissolved in 100 parts of ether, and the solution was washed three times with 50 parts of 2N-sodium hydroxide aqueous solution and extracted three times with 2N-hydrochloric acid aqueous solution. The extract was washed twice with 50 parts of ether and made alkaline by addition of 2N-sodium hydroxide solution. The extraction was conducted three times with 50 parts of ether, and the extract was condensed and distilled under reduced pressure to yield 3.2 parts of 1-(2',3'-dimethylphenyloxy)-3-(tert.-butylamino)-2-propanol having a melting point of 57° C. and a boiling point of 134°-136° C. under 0.7 mm Hg.
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-66d97fab50ce45b5b2f36556e41d0aae |
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| Quellennotiz | uspto-grants-1977_04 |
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