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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733225Generated: October 31, 2026

p-Toluenesulfonic acid → Benzylphthalimide

https://huagongshe.com/reaction/733225

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
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 para-toluenesulfonic 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 numberUS07589117B2
Source datasetuspto-grants-2009_09
ORD IDord-054f7f1643f0470d88905308b285d0dc
Source noteuspto-grants-2009_09