HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839605Generated: October 25, 2026
Acetic Acid → 4-(4-Chlorophenyl)-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/1839605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | 4-(4-Chloro-phenyl)-1H-indole | HCID 22561747 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | t-BuOH ethanol aceticacid | HCID 86587657 | — |
| Product | 4-(4-Chlorophenyl)-1,3-dihydro-indol-2-one | HCID 22561989 | 94% |
Reaction Steps
To the suspension of 4-(4-chloro-phenyl)-1H-indole (1.52 g, 6.68 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (81 mL) was added pyridinium tribromide (90% purity from Aldrich, 7.12 g, 20.0 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (30 mL). Zinc dust was added to the reaction mixture portionwise until the color changed from deep red to light yellow, and the reaction mixture was stirred at room temperature for one hour. The unreacted zinc dust was filtered off and washed with ethanol. The filtrate was concentrated, and the syrupy residue was suspended in water (500 mL) for 0.5 hour. The solid product was precipitated out, filtered, and washed repeatedly with water to remove the zinc salt and pyridine salt. After high vacuum dry, a pure product (1.54 g, 94%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06677368B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-db13ae8ec8e74ef195ffb20f270bd421 |
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| Source note | uspto-grants-2004_01 |
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