HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-Thiobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 85976779 | HCID 85976779 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Thiobenzonitrile | HCID 585058 | 30% |
Reaction Steps
The ethyl 4-cyanophenyl xanthate was dissolved in ethanol (500 ml) and the solution was refluxed. Potassium hydroxide (112 g, 2 m) was added slowly to the resulting hot solution. Thereafter, the reaction mixture solution was refluxed for approximately three hours. The ethanol was distilled off from the reaction mixture and water (100 ml) was added. The reaction mixture was acidified with 6 N sulfuric acid and the reaction product was extracted with ether. The extract was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated and the reaction product was vacuum-distilled to yield 4-cyanobenzenethiol (20 g, 30%), bp 102°-103° C./2 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04424372 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-da30e26ffca04a2e8382f2684c58acc6 |
| Source note | uspto-grants-1984_01 |