HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733225Generated: October 31, 2026
p-Toluenesulfonic acid → Benzylphthalimide
https://huagongshe.com/reaction/733225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Benzylphthalimide | HCID 75059 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589117B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-054f7f1643f0470d88905308b285d0dc |
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| Source note | uspto-grants-2009_09 |
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