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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662983Generated: October 29, 2026

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

https://huagongshe.com/reaction/1662983

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 numberUS08034810B2
Source datasetuspto-grants-2011_10
ORD IDord-5b98cd7be8884c5ea0dc09af7c8184dd
Source noteuspto-grants-2011_10