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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792941Generated: November 2, 2026

p-Toluenesulfonic acid → 3-fluoro-N-isobutylphthalimide

https://huagongshe.com/reaction/1792941

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantIsobutylamineHCID 6558—
Reactant3-Fluorophthalic anhydrideHCID 69551—
SolventTolueneHCID 1140—
Product3-fluoro-N-isobutylphthalimideHCID 22025500—

Reaction Conditions

Temperature140 °C

Reaction Steps

3-Fluoro-N-isobutylphthalimide is prepared as described in Example 2, starting with 3.4 g of 3-fluorophthalic anhydride, 2.0 cm3 of isobutylamine and a catalytic amount of para-toluenesulfonic acid in 20 cm3 of toluene. The reaction mixture is heated at a temperature in the region of 140° C. for 3 hours. After cooling to a temperature in the region of 20° C., the reaction mixture is concentrated to dryness under reduced pressure (2 kPa). The residue is taken up in dichloromethane and washed 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. The residue is dried in a desiccator under reduced pressure (2 kPa) at a temperature in the region of 20° C. 4.0 g of 3-fluoro-N-isobutylphthalimide are thus obtained in the form of an off-white powder. (Rf=0.73, thin layer chromatography on silica gel, eluent: dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078428B2
Source datasetuspto-grants-2006_07
ORD IDord-cbdf2c15a68c4c8bbaa462ea6aa0317e
Source noteuspto-grants-2006_07