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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581701Generated: October 30, 2026

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

https://huagongshe.com/reaction/1581701

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—
Product5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 21905955—
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 of 30 g of 5-chloro-1H-indole-2,3-dione in 250 ml of THF, cooled beforehand in a bath of ice, and the mixture is then left stirring while allowing the temperature to return to RT. After stirring for one hour at RT, the reaction mixture is poured slowly into saturated NH4Cl solution and the THF is evaporated off under vacuum. The precipitate formed is spin-filtered off and washed with iso-ether. 42 g of the expected product are obtained and are used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730695B2
Source datasetuspto-grants-2004_05
ORD IDord-50cc39b169de42a7adf7b963be5c53ad
Source noteuspto-grants-2004_05