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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050458Erstellt: 26. Oktober 2026

Methanesulfonic Acid → Phthalimide

https://huagongshe.com/reaction/1050458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
EduktAcetic AnhydrideHCID 7918—
EduktPhosphorus oxide (P4O10)HCID 14812—
Edukt2-(3-Oxobutyl)isoindoline-1,3-dioneHCID 290728—
LösungsmittelEthyl AcetateHCID 8857—
ProduktPhthalimideHCID 680922,3%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382234B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-86a81e7ba5e140e19d116f530394757f
Quellennotizuspto-grants-2016_07