HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11199Generated: October 27, 2026
Isatin → 1-(4-Methoxyphenyl)indoline-2,3-dione
https://huagongshe.com/reaction/11199
Participants
| Role | Name | HCID | Charge |
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| 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. under a nitrogen atmosphere 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. 4-Bromoanisole (2.13 ml, 1 equivalent) was added followed by copper iodide (6.46 g, 2 equivalents). The reaction was heated in an oil-bath at 145° C. for 7 hours. The reaction was then cooled to room temperature and diluted with an equal volume of ethyl acetate. This suspension was filtered and the filtrate was evaporated to dryness. TLC (1:4, ethyl acetate:hexanes) indicated a very clean reaction; Rf (product)=0.5. The crude material was used as such for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07097995B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-e59131b79bd04d71ba5590af6c25b9b8 |
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| Source note | uspto-grants-2006_08 |
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