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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243323Generated: October 30, 2026

5-chloro-1H-indole-2,3-dione → HCID 21905920, compound

https://huagongshe.com/reaction/1243323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
Reactant1-Bromo-2-(trifluoromethoxy)benzeneHCID 2777266—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21905920HCID 2190592045.8%

Reaction Steps

A solution of 25 g of 1-bromo-2-trifluoromethoxybenzene in 130 ml of ether is added dropwise to a mixture of 2.8 g of magnesium in 20 ml of ether, the reflux being maintained once it has started. At the end of the addition, the mixture is heated at reflux for one hour. A mixture of 7.5 g of 5-chloro-1H-indole-2,3-dione in 100 ml of THF is then added, at a temperature below 40° C., followed by refluxing for one hour. After cooling to RT, the reaction mixture is poured into an ice/concentrated HCl mixture and extracted with EtOAc, the organic phase is washed with water, with 1N NaOH solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 6.5 g of the expected product are obtained after crystallization from a DCM/iso ether mixture (20/80; v/v),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119086B2
Source datasetuspto-grants-2006_10
ORD IDord-f32a143476a94bc4a9881a98c7a3eddc
Source noteuspto-grants-2006_10