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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050458Generated: October 26, 2026

Methanesulfonic Acid → Phthalimide

https://huagongshe.com/reaction/1050458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantAcetic AnhydrideHCID 7918—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant2-(3-Oxobutyl)isoindoline-1,3-dioneHCID 290728—
SolventEthyl AcetateHCID 8857—
ProductPhthalimideHCID 680922.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of acetic anhydride (5.0 mL, 53.0 mmol) and 7.7 wt % phosphorus pentoxide in methanesulfonic acid (Eaton's Reagent) (5.0 mL, 4.60 mmol) was added 2-(3-oxobutyl)isoindoline-1,3-dione (1.0 g, 4.60 mmol). The reaction was heated at 70° C. and for 8 h. The reaction was allowed to cool to room temperature and maintained overnight. The reaction was diluted with EtOAc, washed with ice cold water, dried (Na2SO4), filtered and concentrated under vacuum. The residue was purified by silica gel chromatography (Analogix, SF40-115 g, 20-100% EtOAc in hexanes). The pure fractions were combined and evaporated to dryness and triturated with 10% EtOAc in hexanes, filtered and evaporated to dryness to give 2-(2,6-dimethyl-4-oxo-4H-pyran-3-yl)methyl)isoindoline-1,3-dione (290 mg, 1.024 mmol, 22.24% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 7.91-7.74 (m, 4 H), 6.06 (s, 1 H), 4.54 (s, 2 H), 2.43 (s, 3 H), 2.22 (s, 3 H). MS(ES) [M+H]+ 284.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382234B2
Source datasetuspto-grants-2016_07
ORD IDord-86a81e7ba5e140e19d116f530394757f
Source noteuspto-grants-2016_07