HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443587Generated: October 27, 2026
Hydrochloric Acid → 2,2-Bis(2,2,3,4,4,4-hexafluorobutyl)malononitrile
https://huagongshe.com/reaction/1443587
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,3,4,4,4-Hexafluorobutyl trifluoromethanesulfonate | HCID 58879032 | — |
| Reactant | 2-(2,2,3,4,4,4-Hexafluorobutyl)malononitrile | HCID 86612538 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,2-Bis(2,2,3,4,4,4-hexafluorobutyl)malononitrile | HCID 86612571 | 1.5% |
Reaction Steps
In 50 ml of acetone, 2.0 g of 2-(2,2,3,4,4,4-hexafluorobutyl)malononitrile and 5.3 g of 2,2,3,4,4,4-hexafluorobutyl trifluoromethanesulfonate were dissolved, 1.9 g of potassium carbonate was added and the mixture was stirred at room temperature for 10 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture and the mixture was extracted with t-butyl methyl ether. The organic layer was washed successively with water, aqueous saturated sodium hydrogen carbonate and aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.05 g of 2,2-bis(2,2,3,4,4,4-hexafluorobutyl)malononitrile (hereinafter, referred to as the present compound (95)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662402B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-1345aecfa3a44cb683da51e10c225436 |
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| Source note | uspto-grants-2010_02 |
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