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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385485Generated: October 31, 2026

Phthalic Anhydride → N-Allylphthalimide

https://huagongshe.com/reaction/1385485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantAllylamineHCID 7853—
SolventDimethylformamideHCID 6228—
ProductN-AllylphthalimideHCID 22440198.8%

Reaction Steps

A 500 mL round-bottom flask was charged with phthalic anhydride (22.2 g, 150 mmol) and anhydrous DMF (150 mL) and stirred at room temperature for 5 min to dissolve the phthalic anhydride. To the solution was slowly added allylamine (11.26 mL, 150 mmol) followed by 20 g of 3A molecular sieves. The resulting mixture was stirred at room temperature 10 minutes and then heated under nitrogen at 80° C. for 16 hrs. The reaction mixture was cooled to room temperature and filtered. To the mother liquor was added 300 mL of EtOAc and 300 mL of brine solution. The organic layer was separated, washed twice with 300 mL of water, and dried over MgSO4. The drying agent was removed by filtration and the mother liquor concentrated. The resulting solid was recrystalized from CH2Cl2/hexane to yield 27.75 g (98% yield) of N-allylphthalimide (1-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262268B1
Source datasetuspto-grants-2001_07
ORD IDord-88a93c6d3add4bd5939276fb098166ba
Source noteuspto-grants-2001_07