Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Indole-7-carboxaldehyde | HCID 2734629 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Katalysator | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 7-Ethenyl-1H-indole | HCID 14567404 | — |
Reaktionsschritte
Add potassium tert-butoxide (1 M in tetrahydrofuran, 14.1 mL, 14.1 mmol) to a solution of methyl triphenylphosphonium bromide (5.05 g, 14.1 mmol) in tetrahydrofuran (80 mL) and stir the reaction mixture for 45 minutes at room temperature. Add a solution of 7-formylindole (1.00 g, 6.89 mmol) in tetrahydrofuran (10 mL) and stirred for 1.5 hours. Dilute the reaction mixture with ethyl acetate (250 mL), wash sequentially with an 8:1 mixture of water and 1 N hydrochloric acid (2×100 mL) and saturated aqueous sodium chloride (100 mL), dry over sodium sulfate, filter, and concentrate the filtrate under reduced pressure. Subject the residue silica gel chromatography. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound as a brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08058425B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-26848bd307884ed187f181d62ab4656b |
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| Quellennotiz | uspto-grants-2011_11 |
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