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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 601768Erstellt: 24. Oktober 2026

Iodine → 5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one

https://huagongshe.com/de/reaction/601768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt2-BromoanisoleHCID 11358—
EduktAmmonium ChlorideHCID 25517—
Edukt5-chloro-1H-indole-2,3-dioneHCID 87203—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 2190595589,2%

Reaktionsbedingungen

Temperatur21 °C

Reaktionsschritte

Magnesium turnings (40 g, 1.65 mol) are introduced into diethyl ether (100 ml) and, while stirring, a solution of 2-bromoanisole (206 ml, 1.65 mol) in diethyl ether (450 ml) is added dropwise. The reaction can be initiated, if necessary, by adding iodine crystals. During the addition, the reaction mixture should boil gently. After the addition, the mixture was stirred at room temperature for 1 hour. A slurry of 5-chloroisatin (75 g, 0.41 mol) in THF (750 ml) was added to the Grignard solution while cooling slightly (temperature 18-24° C.), and the mixture was stirred at room temperature for 30 min. The reaction mixture was stirred into ammonium chloride solution and extracted several times with ethyl acetate. The combined organic phase was washed four times with water, dried over magnesium sulfate and concentrated under reduced pressure. The remaining residue was stirred with 2-propanol. The resulting precipitate was filtered off, washed with 2-propanol and diethyl ether and dried. 106 g of the desired intermediate were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902379B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-d27efc37f2e44cfb8528f7a662d313bd
Quellennotizuspto-grants-2011_03