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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040921Generated: October 29, 2026

Phthalimide → 2-(2,2-difluoroethyl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/2040921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantPotassium CarbonateHCID 11430—
ReactantChlorodifluoroethane (mixed isomers)HCID 2736499—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethylformamideHCID 6228—
Product2-(2,2-difluoroethyl)-1H-isoindole-1,3(2H)-dioneHCID 86668440100%

Reaction Conditions

Temperature120 °C

Reaction Steps

An amount of 27.6 g (0.269 mol) of 2,2-difluoro-1-chloroethane, 2.16 g (6.73 mmol) of tetra(n-butyl)ammonium bromide and 20 g (0.135 mol) of phthalimide are dissolved in 95 g of N,N-dimethylformamide and treated with 46.96 g (0.336 mol) of potassium carbonate. The reaction mixture is stirred in an autoclave under pressure at 120° C. for 16 h. After the end of the reaction, cooling is carried out to ambient temperature and the solvent is exhaustively removed under vacuum. The remaining residue is treated with 150 ml of water and the solid is filtered off. The filter residue is washed twice with water and the product is dried under vacuum. An amount of 28.5 g of 2-(2,2-difluoroethyl)-1H-isoindole-1,3(2H)-dione with a purity of 97.4% is obtained. This corresponds to a yield of 97.7% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580973B2
Source datasetuspto-grants-2013_11
ORD IDord-93240e026dcf4615aff1ef2b5f0ec7b9
Source noteuspto-grants-2013_11