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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234481Generated: October 30, 2026

Diethyl Ether → 5-Chloro-1,3-dihydro-3-hydroxy-3-(2-methylphenyl)indol-2-one

https://huagongshe.com/reaction/234481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-BromotolueneHCID 7236—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-1,3-dihydro-3-hydroxy-3-(2-methylphenyl)indol-2-oneHCID 19076469126.4%
ProductHCID 178424303HCID 178424303—

Reaction Steps

A solution of 2-methylphenylmagnesium bromide is prepared from 2.7 g of magnesium, 19 g of 1-bromo-2-methylbenzene and 100 ml of ether. A mixture of 5.04 g of 5-chloroisatin and 100 ml of THF is cooled in an ice bath under an argon atmosphere and the solution of magnesium compound prepared above is added slowly. After stirring for 4 hours, water is added and the solvents are evaporated off under vacuum. The residue is extracted with AcOEt, the precipitate formed is filtered off and the organic phase of the filtrate is dried over magnesium sulfate and evaporated under vacuum. The residue obtained, combined with the precipitate previously filtered off, is crystallized from MeOH to give 4.8 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594023
Source datasetuspto-grants-1997_01
ORD IDord-e1ae98286b044cde9273620f49baa006
Source noteuspto-grants-1997_01