HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54274Generated: October 25, 2026
Potassium Cyanide → 4-(Trifluoromethyl)phenylacetonitrile
https://huagongshe.com/reaction/54274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Trifluoromethyl)phenylacetonitrile | HCID 75359 | 101.3% |
Reaction Steps
A stirred solution of 250.0 grams (1.05 moles) of 4-trifluoromethylphenylmethyl bromide in 1000 mL of ethanol was heated to about 80° C., and a solution of 109.0 grams (1.67 moles) of potassium cyanide in about 275 mL of water was added. Upon completion of addition, the reaction mixture was stirred at 80° C. for about 1.75 hours. After this time the reaction mixture was cooled to ambient temperature and extracted with three portions of diethyl ether. The combined extracts were washed with two portions of water and one portion of an aqueous solution saturated with sodium chloride. The organic layer was added with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding about 197 grams of 4-trifluoromethylphenylacetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05622954 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-5f4e3a2d05c4490fa91de08987a504ef |
|---|
| Source note | uspto-grants-1997_04 |
|---|