HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Hydroxyphthalimide → HCID 13247966, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13247966 | HCID 13247966 | — |
Reaction Steps
(3H-Imidazol-4-yl)-methanol (90 mg, 0.92 mmol) obtained by reducing 3H-imidazole-4-carboaldehyde (commercial product) with lithium aluminum hydride in THF was mixed with PPh3 (245 mg, 0.94 mmol), N-hydroxy-phthalimide (153 mg, 0.94 mmol), and diisopropyl azodicarboxylate (189 mg, 0.94 mmol) in anhydrous THF at 0° C. under a nitrogen atmosphere, and the mixture was stirred. After 4 hours, the reaction mixture was purified by silica gel chromatography to give 2-(3H-imidazol-4-ylmethoxy)-isoindol-1,3-dione (30 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084645B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-42ebbd24de644dd495ed05f2daf20b83 |
| Source note | uspto-grants-2011_12 |