HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443586Generated: October 29, 2026
Hydrochloric Acid → 2,2-Bis(2,2,3,3,3-pentafluoropropyl)malononitrile
https://huagongshe.com/reaction/1443586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,3,3,3-Pentafluoropropyl trifluoromethanesulfonate | HCID 2776019 | — |
| Reactant | 2-(2,2,3,3,3-Pentafluoropropyl)malononitrile | HCID 86612570 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,2-Bis(2,2,3,3,3-pentafluoropropyl)malononitrile | HCID 86612569 | 1.4% |
Reaction Steps
In 20 ml of acetone, 2.1 g of 2-(2,2,3,3,3-pentafluoropropyl)malononitrile and 4.5 g of 2,2,3,3,3-pentafluoropropyl trifluoromethanesulfonate were dissolved, 2.2 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(2,2,3,3,3-pentafluoropropyl)malononitrile (hereinafter, referred to as the present compound (93)).
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-466fcccfdea141f1b76c11f3ccefcd0d |
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| Source note | uspto-grants-2010_02 |
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