HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839629Generated: October 31, 2026
Acetic Acid → 4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/1839629
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | HCID 22561761 | HCID 22561761 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-one | HCID 22561971 | 76% |
Reaction Steps
To the suspension of 4-(2,3-difluoro-phenyl)-1H-indole (2.85 g, 12.4 mmol) in t-BuOH:ethanol:acetic acid (78.5 mL:46.5 mL:24.13 mL) was added pyridinium tribromide (11.93 g, 37.3 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added with acetic acid (60 mL). Zinc dust (4.1 g, 62.2 mmol) was added to the reaction mixture portionwise. After stirring for one hour, any unreacted zinc was filtered off and most of the solvent was removed under reduced pressure. The residue was diluted with ethyl acetate, washed with water (5×), sat NaHCO3, brine, dried over Na2SO4, concentrated and triturated with ether to give 2.32 g (76%) of 4-(2,3-difluoro-phenyl)-1,3-dihydro-indol-2-one as an earth colored solid.
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-2f200598a07347f782b6e0a11a70414f |
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| Source note | uspto-grants-2004_01 |
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