Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,3,3,3-Pentafluoropropyl trifluoromethanesulfonate | HCID 2776019 | — |
| Reactant | (2,2,3,3,4,4,5,5-Octafluoropentyl)propanedinitrile | HCID 25242027 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 15979664 | HCID 15979664 | 2.4% |
Reaction Steps
In 20 ml of acetone, 2.8 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)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 8 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 0.10 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(2,2,3,3,3-pentafluoropropyl)malononitrile (hereinafter, referred to as the present compound (91)).
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-fd938740c8934094b218912d13290f95 |
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| Source note | uspto-grants-2010_02 |
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