Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Tributylvinyltin | HCID 81998 | — |
| Edukt | Lithium Chloride | HCID 433294 | — |
| Edukt | 7-Bromoindole | HCID 2757020 | — |
| Katalysator | Triphenylphosphine | HCID 11776 | — |
| Katalysator | HCID 178479785 | HCID 178479785 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 7-Ethenyl-1H-indole | HCID 14567404 | 80% |
Reaktionsschritte
To 7-bromo-1H-indole (6.0 g, 30.6 mmol) in 150 mL of dimethylformamide was added tributyl(vinyl)tin (9.8 mL, 33.7 mmol), triphenylphosphine (0.4 g, 1.53 mmol), diphenyl-palladium(II) dichloride (1.07 g, 1.53 mmol) and lithium chloride (4.0 g, 94.4 mmol), and the resulting mixture was heated at 100° C. overnight. The reaction mixture was cooled to 20-24° C. and poured into 150 mL of water and 150 mL of ethyl acetate. The aqueous layer was washed with additional ethyl acetate (3×100 mL) and the combined organic layers were washed with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 5-10% ethyl acetate in hexanes. Fractions containing product were combined and concentrated under reduced pressure to provide 3.5 g (80%) of the desired compound as a clear oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06743785B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-0cfbd83475514974a0e7c40b96b6fc3f |
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| Quellennotiz | uspto-grants-2004_06 |
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