HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284681Generated: November 1, 2026
N-methyl-2-pyrrolidone → HCID 90052222, compound
https://huagongshe.com/reaction/2284681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | HCID 90052441 | HCID 90052441 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 90052222 | HCID 90052222 | 75.5% |
Reaction Steps
To 2,2,3-trifluoro-3-(3-nitrophenyl)propyl trifluoromethanesulfonate (C32, 709 mg) and potassium phthalimide (1.07 g), N-methylpyrrolidone (4 mL) was added at room temperature, and the mixture was stirred at 80° C. for 3 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and saturated aqueous sodium hydrogencarbonate were added to the mixture. The organic layer was separated, washed successively with water and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 100 to 30% hexane in ethyl acetate) to obtain 2-(2,2,3-trifluoro-3-(3-nitrophenyl)propyl)isoindoline-1,3-dione (C33, 531 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-772760ac3bb748b0b534c6d0f9b78698 |
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| Source note | uspto-grants-2015_09 |
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