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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219754Erstellt: 24. Oktober 2026

Iodine → 3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-one

https://huagongshe.com/de/reaction/219754

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktAmmonium ChlorideHCID 25517—
Edukt2-BromophenetoleHCID 68500—
Edukt5-IodoisatinHCID 88695—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-oneHCID 57466442—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

4 g (164 mMol) of magnesium turnings and 5% of the total amount of 2-bromo-1-ethoxybenzene were put into 20 ml of ether and, after addition of a little iodine, were heated until the reaction started. 33.1 g (165 mMol) of 2-bromo-1-ethoxybenzene dissolved in 100 ml of ether were slowly added dropwise to the boiling solution in such a way that the reaction continued with gentle boiling. Then, while cooling slightly to 20° C., 15 g (54.9 mMol) of 5-iodoisatin in 400 ml of anhydrous tetrahydrofuran were added dropwise. The mixture was then stirred at room temperature for 2 h. The reaction solution was poured into an aqueous NH4Cl solution with stirring. This aqueous phase was extracted several times with ethyl acetate, and the combined aqueous phase was washed four times with water, dried and concentrated in vacuo, resulting in the product as a crystalline precipitate. 19.2 g of the product were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202870B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f588b2f796754e5b9d1ed63240c9f62f
Quellennotizuspto-grants-2012_06