HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191411Generated: November 3, 2026
Acetic Acid → 4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/2191411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | HCID 22561761 | HCID 22561761 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-one | HCID 22561971 | 97% |
Reaction Steps
4-(2,3-difluoro-phenyl)-1H-indole 6c (744 mg, 3.25 mmol) was dissolved in 12 ml of ethanol under stirring, and added successively with tert-butanol (21 ml), glacial acetic acid (6.4 ml) and pyridinium tribromide (3.12 g, 9.7 mmol) at room temperature. Upon completion of the addition, the reaction mixture was stirred for 3 hours, added with glacial acetic acid (16 ml) and zinc dust (1.1 g, 16.25 mmol), and stirred for another 1 hour. The reaction mixture was filtered and concentrated under reduced pressure. The residue was added with ethyl acetate (30 ml), washed successively with water (10 ml), saturated sodium bicarbonate solution (10 ml) and saturated brine (10 ml), dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure to obtain 4-(2,3-difluoro-phenyl)-1,3-dihydro-indol-2-one 6d (780 mg, yield 97%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08329682B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-6b99baa547f94c3798ae719d931084f7 |
|---|
| Source note | uspto-grants-2012_12 |
|---|