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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 1-(3,5-Dichlorophenyl)-1H-indole | HCID 18474808 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Phosphoric Acid | HCID 1004 | — |
| Product | 1-(3,5-Dichlorophenyl)-1,3-dihydro-indol-2-one | HCID 18474811 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06414153B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-18ee8d4217ce416cafbbbc762f076cd1 |
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| Source note | uspto-grants-2002_07 |
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