HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 3-Bromo-6-(phenylthio)-phenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Bromo-6-(phenylthio)-benzyl chloride | HCID 21456037 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-6-(phenylthio)-phenylacetonitrile | HCID 21481134 | — |
Reaction Steps
136.5 g of potassium cyanide in 183 ml of water are heated under reflux for 10 hours under a nitrogen atmosphere with 470 g of 3-bromo-6-(phenylthio)-benzyl chloride. The ethanol is distilled off under reduced pressure, the residue diluted with water and extracted with ether. The extracts are washed with water, dried over magnesium sulphate and evaporated. There is obtained 3-bromo-6-(phenylthio)-phenylacetonitrile as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006144 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-663544e8b1624638ab6c5cbb787c4e51 |
| Source note | uspto-grants-1977_02 |