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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium BicarbonateHCID 516892—
ReactantPhthalimide potassium saltHCID 24194345—
ReactantHCID 90052441HCID 90052441—
SolventEthyl AcetateHCID 8857—
ProductHCID 90052222HCID 9005222275.5%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-772760ac3bb748b0b534c6d0f9b78698
Source noteuspto-grants-2015_09