HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → 3-(3-(1,3-Dioxoisoindolin-2-yl)propyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | 3-(3-(1,3-Dioxoisoindolin-2-yl)propyl)benzaldehyde | HCID 57766465 | — |
Reaction Steps
To a solution of phthalimide 50 (5.66 g, 16.67 mmol) in acetone-water (5:1, 50 mL) was added p-toluenesulfonic acid hydrate (0.2116 g, 1.11 mmol). The mixture was stirred for 3 h then concentrated under reduced pressure. The residue was partitioned between EtOAc and water and the combined organics were washed with brine, dried over MgSO4 and concentrated under reduced pressure to give phthalimide 29 as a white solid. Yield (4.48 g, 92%). The NMR data was consistent with data reported above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653142B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-73db8925cdd745cb8738b9bd8b6da10e |
| Source note | uspto-grants-2014_02 |