HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium thiocyanate → 1-(alpha-Thiocyanoacetyl) azetidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 1-(Azetidin-1-yl)-2-chloroethan-1-one | HCID 2543159 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(alpha-Thiocyanoacetyl) azetidine | HCID 53670774 | — |
Reaction Steps
1-(α-Chloroacetyl) azetidine (13 grams; 0.1 mol), potassium thiocyanate (18 grams; 0.18 mol) and ethanol (100 ml) are charged into a glass reaction flask equipped with stirrer and reflux condenser. The reaction mixture is then heated at reflux, with stirring, for a period of about 4 hours. After this time the reaction mixture is cooled and filtered. The filtrate is then stripped of ethanol leaving a residue. The residue is extracted twice with hot benzene and the two benzene extracts are combined. The benzene extract is then evaporated under reduced pressure to yield 1-(α-thiocyanoacetyl) azetidine as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998808 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-d16fa4394c0e450db58adfab8008724e |
| Source note | uspto-grants-1976_12 |