HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649988Generated: October 25, 2026
2-bromo-N-(2,6-dimethylphenyl)butanamide → N-(2-phthalimido-butyryl)-2,6-dimethyl-aniline
https://huagongshe.com/reaction/1649988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-bromo-N-(2,6-dimethylphenyl)butanamide | HCID 13010804 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-phthalimido-butyryl)-2,6-dimethyl-aniline | HCID 19855569 | 71.1% |
Reaction Steps
A mixture of 20.0 g (74 mmoles) of N-(2-bromo-butyryl)--2,6-dimethyl-aniline, 27.8 g (0.15 moles) of potassium phthalimide and 150 ml of dry dimethyl formamide is stirred at 60° C. for 2 hours. The mixture is cooled, poured onto 750 ml of ice water, the separated crystalline substance is filtered off, washed with water and dried. The resulting crude product, weighing 35.7 g, is dissolved in 200 ml of chloroform, the solution is washed thrice with 50 ml of 1 n aqueous sodium hydroxide solution and thrice with 50 ml of water, each, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure. 17.7 g (71.1%) of N-(2-phthalimido-butyryl)-2,6-dimethyl-aniline are obtained; m.p.: 195°-196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04922021 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-8a7fddd1c6384d6eae1912f0f7b9ff2e |
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| Source note | uspto-grants-1990_05 |
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