HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Nitroanisole → 7-methoxy-2-methyl-1H-indole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Nitroanisole | HCID 7048 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178456138 | HCID 178456138 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 7-methoxy-2-methyl-1H-indole | HCID 326614 | — |
Reaktionsschritte
800 ml of a 0.5M solution of isopropenylmagnesium bromide in THF is cooled to −40° C. under a nitrogen atmosphere, a solution of 20.4 g of 2-methoxynitrobenzene in 125 ml of THF is then added dropwise and the mixture is left stirring for 1 hour while allowing the temperature to return to 0° C. The reaction mixture is poured into a saturated NH4Cl solution and extracted with ether, the organic phase is washed with a saturated NaCl solution and dried over MgSO4, and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, elution being carried out with cyclohexane and then with a cyclohexane/EtOAc mixture (90/10; v/v). 2.45 g of the expected compound are obtained in the form of an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07741363B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-0c8cf4b31c33475abf246acdc409da3c |
| Quellennotiz | uspto-grants-2010_06 |