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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601768Generated: October 25, 2026

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

https://huagongshe.com/reaction/601768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-BromoanisoleHCID 11358—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 2190595589.2%

Reaction Conditions

Temperature21 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902379B2
Source datasetuspto-grants-2011_03
ORD IDord-d27efc37f2e44cfb8528f7a662d313bd
Source noteuspto-grants-2011_03