HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506429Generated: October 26, 2026
Isatin → 1-(4-Methoxyphenyl)indoline-2,3-dione
https://huagongshe.com/reaction/506429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-Methoxyphenyl)indoline-2,3-dione | HCID 13925094 | — |
Reaction Steps
A solution of isatin (2.5 g, 0.017 mol) in anhydrous DMF (50 mL) was cooled to 0° C. in an ice-bath and treated with sodium hydride (0.5 g, 1.2 equivalents). A purple solution was formed which was stirred at 0° C. for 30 minutes and then warmed to room temperature. To this solution was added 4-bromoanisole (2.13 mL, 1 equivalent) followed by copper iodide (6.46 g, 2 equivalents). The reaction was heated in an oil-bath at 145° C. for 6-7 hours. The reaction was then cooled to room temperature, diluted with an equal volume of ethyl acetate and filtered. The filtrate was evaporated to dryness. The crude product, which was obtained as a dark brown solid was used as such for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07785904B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-658a8f8643c94eacbbd5e4d286e934a1 |
|---|
| Source note | uspto-grants-2010_08 |
|---|