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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1243317Erstellt: 25. Oktober 2026

Iodine → 5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1243317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt2-BromoanisoleHCID 11358—
EduktMagnesiumHCID 5462224—
Edukt5,6-dichloro-1H-indole-2,3-dioneHCID 11009341—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 2192550280,6%

Reaktionsschritte

7.5 g of 1-bromo-2-methoxybenzene are added dropwise to a suspension of 1.1 g of magnesium in 20 ml of ether containing a few crystals of iodine, the reflux being maintained once it has started. At the end of the addition, the mixture is heated at reflux for 2 hours. A suspension of 4.3 g of 5,6-dichloro-1H-indole-2,3-dione in 20 ml of THF is then added and the resulting mixture is refluxed for 30 minutes. After cooling to RT, the reaction mixture is poured into a water/ice/concentrated HCl mixture and extracted with EtOAc, the organic phase is dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is triturated in hot iso ether and the precipitate formed is filtered off by suction and washed with ether. 5.2 g of the expected product are obtained, m.p.=245–246° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07119086B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-565d91cc6fda462198d18bd8a8f68e27
Quellennotizuspto-grants-2006_10