HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → p-(1-Chloroethyl)phenyl 2-thienyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | p-(1-Hydroxyethyl)phenyl 2-thienyl ketone | HCID 12232927 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | p-(1-Chloroethyl)phenyl 2-thienyl ketone | HCID 12232928 | — |
Reaction Steps
To a stirred and cooled solution of 43.7 parts of p-(1-hydroxyethyl)phenyl 2-thienyl ketone in 180 parts of dry benzene are added dropwise 16 parts of thionyl chloride. Upon completion, stirring is continued overnight at room temperature. The reaction mixture is evaporated. The residue is taken up in toluene and the latter is evaporated once more. The latter residue is distilled and the distillate is crystallized from ethanol at room temperature, yielding p-(1-chloroethyl)phenyl 2-thienyl ketone; mp. 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064132 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-e836e8cff79f468099b325e1392aaf62 |
| Source note | uspto-grants-1977_12 |