HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31352Erstellt: 23. Oktober 2026
2-Bromoanisole → 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one
https://huagongshe.com/de/reaction/31352
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromoanisole | HCID 11358 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dione | HCID 2732752 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one | HCID 21905899 | 76,3% |
| Produkt | HCID 178489560 | HCID 178489560 | — |
Reaktionsschritte
A solution of 2-methoxyphenylmagnesium bromide is prepared starting with 1.9 g of magnesium in 4 ml of ether and a solution of 14.54 g of 1-bromo-2-methoxybenzene in 21 ml of ether. This solution is added dropwise, under an argon atmosphere, to a mixture of 5 g of 5-trifluoromethoxy-1H-indole-2,3-dione in 26 ml of THF, precooled on an ice bath, the resulting mixture is then heated at the reflux temperature of the ether for 1 hour 30 minutes and is allowed to cool to RT. The reaction mixture is poured slowly into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with 5% K2CO3 solution, with water and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425566B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-c0c9fcda8b5943aea3d4da63af3bb7f5 |
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| Quellennotiz | uspto-grants-2008_09 |
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