HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805131Generated: October 25, 2026
Succinic anhydride → 4-[(2-Tert-butylphenyl)amino]-4-oxobutanoic acid
https://huagongshe.com/reaction/1805131
Participants
| Role | Name | HCID | Charge |
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| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | 2-tert-Butylaniline | HCID 80574 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[(2-Tert-butylphenyl)amino]-4-oxobutanoic acid | HCID 6468356 | — |
Reaction Steps
To a solution of 2-tert-butylaniline (1.0 g, 6.7 mmol) in toluene (15 mL) was added tetrahydrofuran-2,5-dione (0.81 g, 8.1 mmol) and the reaction mixture was refluxed for 1 h. The reaction mixture was cooled and filtered to obtain 4-(2-tert-butylphenylamino)-4-oxobutanoic acid, which was dissolved in acetic acid (20 mL) and sodium acetate (3.02 g, 36.86 mmol) and was stirred at 80° C. overnight. The reaction was quenched with water, the layers separated and the aqueous layer was extracted with DCM. The combined organic layer was dried over MgSO4, filtered and concentrated. The resulting solid was recrystallized from ethanol, to obtain pure 1-(2-tert-butylphenyl)pyrrolidine-2,5-dione (930 mg, 60%). LC/MS: m/z 232.3 (M+H)+ at 1.264 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354427B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-27602b7047e14a4e891deee1edf295c3 |
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| Source note | uspto-grants-2013_01 |
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