Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Isatin | HCID 7054 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(3-Bromophenyl)-1,3-dioxolane | HCID 87306 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[3-(1,3-dioxolyl)phenyl]isatin | HCID 21972258 | — |
Reaction Steps
Isatin (3.2 g, 0.0218 moles) was dissolved in anhydrous DMF (75 mL) and cooled in an ice bath under a nitrogen atmosphere. To this cold solution, sodium hydride (0.575 g, 0.0239 moles) was added and the reaction was stirred at 0° C. for 1.5 hours. This solution was then treated with 2-(3-bromophenyl)-1,3-dioxolane (5 g, 1 equivalent) followed by CuI (8.3 g, 2 equivalents). The resulting suspension was heated in an oil-bath under nitrogen at 130-140° C. for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. This suspension was filtered and the filtrate was concentrated under reduced pressure. A viscous brown oil was recovered which was suspended in a xylenes (150 mL) wand evaporated to dryness. The residue was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion; Rf (product)=0.86.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07611909B1 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-a832cacbd4894615a14088b86f00fefb |
|---|
| Source note | uspto-grants-2009_11 |
|---|