HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Fluoro-2-methylphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-(Chloromethyl)-4-fluoro-1-methylbenzene | HCID 20511795 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Fluoro-2-methylphenylacetonitrile | HCID 2774625 | — |
Reaction Steps
To a stirred and refluxing mixture of 71 parts of sodium cyanide, 99 parts of ethanol and 85 parts of water is added dropwise a solution of 134 parts of 2-(chloromethyl)-4-fluoro-1-methylbenzene in 99 parts of ethanol. Upon completion, stirring is continued first for 6 hours at reflux and further overnight at room temperature. The ethanol is evaporated and the residue is taken up in 4-methyl-2-pentanone and water. The layers are separated and the aqueous phase is extracted three times with 4-methyl-2-pentanone. The combined organic phases are washed twice with water, dried, filtered and evaporated. The residue is distilled, yielding 98 parts of 5-fluoro-2-methylbenzeneacetonitrile; bp. 124°-128° C. at 10 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369184 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-b26319d057a441ac921d0da957646c3a |
| Source note | uspto-grants-1983_01 |