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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227795Generated: October 26, 2026

Diethyl Ether → 1-(3,5-Dichlorophenyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2227795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantChlorosuccinimideHCID 31398—
Reactant1-(3,5-Dichlorophenyl)-1H-indoleHCID 18474808—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventPhosphoric AcidHCID 1004—
Product1-(3,5-Dichlorophenyl)-1,3-dihydro-indol-2-oneHCID 1847481171%

Reaction Steps

To a solution of 7.8 g (29.9 mmol) of 1-(3,5-Dichlorophenyl)-1H-indole in 50 mL of acetic acid was added 4.0 g (30.1 mmol) of N-chlorosuccinimide. The mixture was warmed at reflux for 1hr, when TLC indicated the disappearance of starting material. The mixture was cooled and diluted with 16 mL of 70% aqueous phosphoric acid and 4 mL of water and warmed at reflux for 6 hr. The reaction was then cooled to afford a precipitate which was diluted with 50 mL of water and collected by filtration. The solid was partially dried by pulling vacuum through the filter cake and then dissolved in dichloromethane, dried (MgSO4), treated with carbon (Norit A), filtered through diatomaceous earth and concentrated to afford an orange solid. Trituration with ether gave 5.9 g (71%) of 1-(3,5-dichlorophenyl)-1,3-dihydro-indol-2-one which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414153B1
Source datasetuspto-grants-2002_07
ORD IDord-18ee8d4217ce416cafbbbc762f076cd1
Source noteuspto-grants-2002_07