HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443588Generated: October 25, 2026
Hydrochloric Acid → 2-(3,3,4,4,5,5,5-Heptafluoropentyl)-2-(2,2,3,3,3-pentafluoropropyl)malononitrile
https://huagongshe.com/reaction/1443588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Alkyl iodides, C4-20, gamma-omega-perfluoro | HCID 109697 | — |
| Reactant | 2-(2,2,3,3,3-Pentafluoropropyl)malononitrile | HCID 86612570 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(3,3,4,4,5,5,5-Heptafluoropentyl)-2-(2,2,3,3,3-pentafluoropropyl)malononitrile | HCID 58879049 | 0.8% |
Reaction Steps
In 50 ml of acetone, 3.2 g of 2-(2,2,3,3,3-pentafluoropropyl)malononitrile and 7.2 g of 5-iodo-1,1,1,2,2,3,3-heptafluoropentane were dissolved, 3.2 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-(3,3,4,4,5,5,5-heptafluoropentyl)-2-(2,2,3,3,3-pentafluoropropyl)malononitrile (hereinafter, referred to as the present compound (96)):
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-eefc2ac2d1244872bf884ea02f262c29 |
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| Source note | uspto-grants-2010_02 |
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