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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792915Generated: November 4, 2026

Phthalic Anhydride → Benzylphthalimide

https://huagongshe.com/reaction/1792915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantBenzylamineHCID 7504—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
ProductBenzylphthalimideHCID 75059—

Reaction Conditions

Temperature140 °C

Reaction Steps

N-Benzylphthalimide is prepared as described in Example 2, starting with 10 g of phthalic anhydride, 7.3 cm3 of benzylamine and a catalytic amount of paratoluenesulfonic acid in 100 cm3 of toluene. The reaction mixture is heated at a temperature in the region of 140° C. for 3 hours and is then cooled to a temperature in the region of 20° C. The reaction mixture is taken up in 100 cm3 of saturated aqueous sodium bicarbonate solution and the aqueous phase is extracted twice with 100 cm3 of ethyl acetate. The organic extracts are combined, washed with 50 cm3 of brine, dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue is dried in a desiccator under reduced pressure (2 kPa) at a temperature in the region of 20° C. 10.3 g of N-benzylphthalimide are thus obtained in the form of a white powder. (Rf=0.44, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (75/25 by volume)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078428B2
Source datasetuspto-grants-2006_07
ORD IDord-660e8600ee76448898112dcc0dde93fb
Source noteuspto-grants-2006_07