HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733260Generated: October 25, 2026
p-Toluenesulfonic acid → N-isobutyl-3-methylphthalimide
https://huagongshe.com/reaction/733260
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 4-Methyl-1,3-isobenzofurandione | HCID 98500 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-isobutyl-3-methylphthalimide | HCID 22025457 | — |
Reaction Steps
N-Isobutyl-3-methylphthalimide is prepared as described in Example 2, starting with 5.0 g of 3-methylphthalic anhydride, 3.0 cm3 of isobutylamine and a catalytic amount of para-toluenesulfonic acid in 50 cm3 of toluene. The reaction mixture is heated at a temperature in the region of 140° C. for 2.5 hours and then stirred at a temperature in the region of 20° C. for 16 hours. The reaction mixture is concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue is taken up in dichloromethane and washed twice with saturated aqueous sodium bicarbonate solution. The organic phase is separated out after settling has taken place, dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. 6.0 g of N-isobutyl-3-methylphthalimide are thus obtained in the form of a caramel-colored oil, Rf=0.76 (thin layer chromatography on silica gel, eluent: dichloromethane).
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-952dde3d152447d9bb281d8fcc8ee311 |
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| Source note | uspto-grants-2009_09 |
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