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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantIsobutylamineHCID 6558—
Reactant4-Methyl-1,3-isobenzofurandioneHCID 98500—
SolventTolueneHCID 1140—
ProductN-isobutyl-3-methylphthalimideHCID 22025457—

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589117B2
Source datasetuspto-grants-2009_09
ORD IDord-952dde3d152447d9bb281d8fcc8ee311
Source noteuspto-grants-2009_09