Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178418507 | HCID 178418507 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6,7-dichloro-1H-indole | HCID 12272802 | — |
Reaktionsschritte
800 ml of a 1M solution of vinylmagnesium bromide in THF are cooled to −45° C. under a nitrogen atmosphere, a solution of 51.2 g of 2,3-dichloronitrobenzene in 1000 ml of THF is then added dropwise and the mixture is left stirring at −30° C. for 1 hour. The reaction mixture is poured onto 1000 ml of a saturated NH4Cl solution and extracted with ether, the combined organic phases are washed with water and with a saturated NaCl solution and dried over MgSO4, and the solvents are evaporated under vacuum. The residue is chromatographed on silica gel, elution being carried out with a cyclohexane/EtOAc mixture (95/5; v/v). 27.75 g of the expected compound are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741363B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-20708af8b784463d960ef216aa77f69e |
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| Quellennotiz | uspto-grants-2010_06 |
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