HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733257Generated: October 25, 2026
p-Toluenesulfonic acid → 3,6-difluoro-N-isobutylphthalimide
https://huagongshe.com/reaction/733257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 3,6-Difluorophthalic anhydride | HCID 513918 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,6-difluoro-N-isobutylphthalimide | HCID 22025417 | — |
Reaction Steps
3,6-Difluoro-N-isobutylphthalimide is prepared as described in Example 2, starting with 5.0 g of 3,6-difluorophthalic anhydride, 2.7 cm3 of isobutylamine and a catalytic amount of para-toluenesulfonic acid in 50 cm3 of toluene. The reaction mixture is refluxed for 3 hours. After cooling to a temperature in the region of 20° C., the reaction mixture is filtered and then concentrated to dryness under reduced pressure (2 kPa). The residue is taken up in 50 cm3 of saturated aqueous sodium bicarbonate solution and washed 3 times with 80 cm3 of dichloromethane. The organic extracts are combined, dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. 6.41 g of 3,6-difluoro-N-isobutylphthalimide are thus obtained in the form of a pale yellow solid. (Rf=0.74, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (50/50 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-683685711d734bb8b0976c051a2d29bb |
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| Source note | uspto-grants-2009_09 |
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