HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443584Generated: October 29, 2026
Hydrochloric Acid → 2-(4,4,5,5,5-Pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrile
https://huagongshe.com/reaction/1443584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3,3,3-Trifluoropropyl)malononitrile | HCID 22185761 | — |
| Reactant | 4,4,5,5,5-Pentafluoropentyl trifluoromethanesulfonate | HCID 86612567 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(4,4,5,5,5-Pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrile | HCID 86612568 | 20.4% |
Reaction Steps
To 10 ml of ethylene glycol dimethyl ether, 6.2 g of 4,4,5,5,5-pentafluoropentyl trifluoromethanesulfonate, 1.6 g of 2-(3,3,3-trifluoropropyl)malononitrile and 1.4 g of potassium carbonate were added and the mixture was stirred at room temperature for 5 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 0.65 g of 2-(4,4,5,5,5-pentafluoropentyl)-2-(3,3,3-trifluoropropyl)malononitrile (hereinafter, referred to as the present compound (89)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07662402B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-d282432eb6f94f90a9b13acc5b63d3c3 |
|---|
| Source note | uspto-grants-2010_02 |
|---|