HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → alpha-Chloro-p-tolyl 2-thienyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | alpha-Hydroxy-p-tolyl 2-thienyl ketone | HCID 21391792 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | alpha-Chloro-p-tolyl 2-thienyl ketone | HCID 21391736 | — |
Reaction Steps
To a stirred and cooled suspension of 31 parts of α-hydroxy-p-tolyl 2-thienyl ketone in 160 parts of dry benzene are added dropwise 24 parts of thionyl chloride at 10° C. Upon completion, stirring is continued overnight at room temperature. The reaction mixture is evaporated and the residue is evaporated twice more from toluene. The latter residue is triturated in petroleumether. The product is filtered off and dissolved in 320 parts of ether. This solution is stirred with charcoal, filtered and the filtrate is evaporated. The residue is crystallized from ethanol at -20° C, yielding α-chloro-p-tolyl 2 -thienyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064132 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-0a63a6d00ba049ebbac099dcd1dee036 |
| Source note | uspto-grants-1977_12 |