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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358476Generated: November 1, 2026

Diethyl Ether → 3,5-Dichloro-3-(2-methoxyphenyl)indolin-2-one

https://huagongshe.com/reaction/1358476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-BromoanisoleHCID 11358—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3,5-Dichloro-3-(2-methoxyphenyl)indolin-2-oneHCID 21905913—
ProductHCID 178489560HCID 178489560—

Reaction Steps

This compound is prepared according to the procedure disclosed in WO 95/18105. A solution of 2-methoxyphenylmagnesium bromide is prepared from 16 g of magnesium in 35 ml of ether and from a solution of 124 g of 1-bromo-2-methoxybenzene in 175 ml of ether. This solution is added dropwise under an argon atmosphere to a mixture, cooled beforehand in an ice bath, of 30 g of 5-chloro-1H-indole-2,3-dione in 250 ml of THF and then the mixture is left stirring while allowing the temperature to rise to AT. After stirring for 1 hour at AT, the reaction mixture is slowly poured onto a saturated NH4Cl solution and the THF is evaporated under vacuum. The precipitate formed is filtered off and is washed with iso ether. 42 g of the expected product are obtained, which product is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596732B2
Source datasetuspto-grants-2003_07
ORD IDord-4fb6124f230944098d54b931395e7b7b
Source noteuspto-grants-2003_07