HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Carbethoxyphthalimide → Phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Phthalimide | HCID 6809 | — |
Reaction Steps
To a stirred solution of 4-aminobutyraldehyde diethyl acetal 1a (89.3 mmol) in CH3CN (100 mL) was added N-carbethoxyphthalimide (93.8 mmol). Once the reaction was complete, the acetonitrile was removed under reduced pressure and the aqueous phase extracted with EtOAc (×3). The organic phase were combined, then washed with water (×4), saturated brine (×3), then dried (Na2SO4), filtered, and evaporated under reduced pressure to give the title compound 1b, which crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855295B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ece6f6c5ad2f44a69b4ba65e5c1c1976 |
| Source note | uspto-grants-2010_12 |