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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722455Generated: October 30, 2026

2-Methoxypropene → 2-(1-Methoxy-1-methylethoxy)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/722455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxypropeneHCID 8300—
ReactantN-HydroxyphthalimideHCID 10665—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product2-(1-Methoxy-1-methylethoxy)-1H-isoindole-1,3(2H)-dioneHCID 1360820775.5%

Reaction Steps

To a solution of 20 g (123 mmol) of N-hydroxyphthalimide in 360 ml of CH3CN, 26.42 ml (276 mmol) of 2-methoxypropene and 42.36 mg (0.246 mmol) of anhydrous p-toluenesulfonic acid are added in portions at r.t. After stirring for 1 h, the mixture is diluted with 25 ml of sat. NaHCO3 and concentrated under reduced pressure. The residue is extracted with EtOAc and the organic layer is washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure to give 21.84 g of 2-(1-methoxy-1-methyl-ethoxy)isoindole-1,3-dione as a white solid; NMR (CDCl3): 1.57 (s, 6H), 3.61 (s, 3H), 7.75 (dd, 2H, J=5.56 Hz, J=3.0 Hz), 7.83 (dd, 2H, J=5.56 Hz, J=3.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138432B1
Source datasetuspto-grants-2006_11
ORD IDord-0a5213ece4f94f71bba85e7d0e1a592d
Source noteuspto-grants-2006_11