HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040927Generated: October 31, 2026
Potassium Carbonate → HCID 86668441, compound
https://huagongshe.com/reaction/2040927
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Chlorodifluoroethane (mixed isomers) | HCID 2736499 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86668441 | HCID 86668441 | 88.1% |
Reaction Steps
An amount of 40.9 g (0.39 mol) of 2,2-difluoro-1-chloroethane, 3.22 g (9.9 mmol) of tetra(n-butyl)ammonium bromide, 95 g of N,N-dimethylformamide and 20 g (0.19 mol) of succinimide are treated with 83.6 g (0.599 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 reaction mixture is subsequently filtered. The filter residue is washed with dichloromethane and the solvent is removed under vacuum. The oil is once more treated with 30 ml of water and extracted twice with 30 ml of dichloromethane. The combined organic phases are dried and the solvent is removed under vacuum. An amount of 27.3 g of 1-(2,2-difluoroethyl)pyrrolidine-2,5-dione with a purity of 93% is obtained. This corresponds to a yield of 77.8% 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-6b12818571bf429c8d7d8c3af895b4ec |
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| Source note | uspto-grants-2013_11 |
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