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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733234Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 4126466, compound

https://huagongshe.com/reaction/733234

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantIsobutylamineHCID 6558—
Reactant4-Chlorophthalic anhydrideHCID 67044—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
ProductHCID 4126466HCID 4126466—

Reaction Conditions

Temperature140 °C

Reaction Steps

4-Chloro-N-isobutylphthalimide is prepared as described in Example 2, starting with 10 g of 4-chlorophthalic anhydride, 5.4 cm3 of isobutylamine 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 16 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. 12 g of 4-chloro-N-isobutylphthalimide are thus obtained in the form of a white powder. (Rf=0.85, 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-eafd6003e1bd4126a373cf9299b4c1c5
Source noteuspto-grants-2009_09