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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chlorodifluoroethane (mixed isomers) | HCID 2736499 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2,2-difluoroethyl)-1H-isoindole-1,3(2H)-dione | HCID 86668440 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580973B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-93240e026dcf4615aff1ef2b5f0ec7b9 |
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| Source note | uspto-grants-2013_11 |
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