HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Biphenyl-3-yl-1,3-dihydro-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | 4-biphenyl-3-yl-1H-indole | HCID 22561802 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-Biphenyl-3-yl-1,3-dihydro-indol-2-one | HCID 22561692 | 72% |
Reaction Steps
To the suspension of 4-bipheny-3-yl-1H-indole (3.5 g, 13 mmol) in t-BuOH:ethanol:acetic acid (82 mL:49 mL:269 mL) was added pyridinium tribromide (12.7 g, 40 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added acetic acid (63 mL). Zinc dust (4.39 g, 67 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 (3×), sat. NaHCO3, brine, dried over Na2SO4, concentrated and triturated with ether to give 2.67 g (72%) of 4-biphenyl-3-yl-1,3-dihydro-indol-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06677368B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-a2c52ea628d748d48712ccb9171fff43 |
| Source note | uspto-grants-2004_01 |