HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Phenacyl thiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2'-Bromoacetophenone | HCID 75060 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Water | HCID 962 | — |
| Product | Phenacyl thiocyanate | HCID 219693 | — |
Reaction Steps
In accordance with the known process (Beilstein, 8, 94), 10.0 g (50 mmol) of o-bromoacetophenone and 4.9 g (50 mmol) of potassium thiocyanate were added to 80 ml of ethyl alcohol, and the resultant mixture was heated at 80° C. for 3 hours and then allowed to stand overnight. Added to the reaction mixture were 50 ml of water. Precipitated crystals were collected by filtration, washed with 50% aqueous ethyl alcohol and then dried, whereby the title compound was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112841 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-89cd3467c1aa4bdf84dd26db3d3a38a0 |
| Source note | uspto-grants-1992_05 |