HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21481140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 818027 | HCID 818027 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21481140 | HCID 21481140 | — |
Reaction Steps
230 g of 3-nitro-6-(phenylthio)-benzyl chloride, 540 ml of ethanol and 320 ml of dioxane are treated with a solution of 70.5 g of potassium cyanide in 150 ml of water. The mixture is heated to reflux for 3 hours and subsequently concentrated under reduced pressure. The residue is diluted with water and extracted with benzene. The organic phase is washed with water and evaporated under reduced pressure. There is obtained 3-nitro-6-(phenylthio)-phenylacetonitrile as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006145 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-c624ebb4444a4f9e92761248656d5e62 |
| Source note | uspto-grants-1977_02 |