Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Phenylindole | HCID 96502 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Produkt | 3-phenyl-2,3-dihydro-1H-indole | HCID 10932353 | — |
Reaktionsschritte
1.3 G of 3-phenylindole was suspended in 100 ml of 20% aqueous hydrochloric acid. The mixture was heated to 60° C. while stirring vigorously and 20 g of zinc dust was added thereto in small portions over a period of 45 minutes. On completing the addition of zinc dust, the reaction mixture was heated to 100° C. and maintained at this temperature for one hour, filtered hot, and the filtrate cooled to room temperature and washed with ether. The aqueous layer was basified with 50% aqueous sodium hydroxide and the desired product was extracted with ether and then purified by column chromatography using silica gel. The 3-phenylindoline was obtained in a yield of 0.8 g as a yellow viscous oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04153789 |
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| Quelldatensatz | uspto-grants-1979_05 |
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| ORD ID | ord-408e9a76d31647578c20129546c09678 |
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| Quellennotiz | uspto-grants-1979_05 |
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