HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → m-Trifluoromethylphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3-(Trifluoromethyl)benzyl chloride | HCID 69716 | — |
| Solvent | Water | HCID 962 | — |
| Product | m-Trifluoromethylphenylacetonitrile | HCID 75360 | 107.1% |
Reaction Steps
A mixture of 12.0 g (61.5 mmole) m-trifluoromethylbenzyl chloride, 9.56 g (195 mmole) sodium cyanide and 60 ml dimethylsulfoxide was heated at 50° to 80° C. for four hours and poured into water. The aqueous mixture was extracted with methylene chloride, the extracts dried over sodium sulfate and the solvent evaporated in vacuo to give 12.2 g of yellow oil which was used in the next step. 1H-NMR(CDCl3)ppm(delta): 3.80 (s, 2H), 7.60 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560690 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-d46f14b90c1e453ea64887a24298fe1f |
| Source note | uspto-grants-1985_12 |