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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264885Generated: November 1, 2026

N-Carbethoxyphthalimide → Phthalimide

https://huagongshe.com/reaction/2264885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-CarbethoxyphthalimideHCID 31187—
Reactant4,4-DiethoxybutylamineHCID 80672—
SolventAcetonitrileHCID 6342—
ProductPhthalimideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855295B2
Source datasetuspto-grants-2010_12
ORD IDord-ece6f6c5ad2f44a69b4ba65e5c1c1976
Source noteuspto-grants-2010_12