HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21391745, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21391763 | HCID 21391763 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21391745 | HCID 21391745 | — |
Reaction Steps
5.5 parts of thionyl chloride is added dropwise to a stirred solution of 9.5 parts of α-hydroxy-α-methyl-m-tolyl 2-thienyl ketone in 40 parts of benzene while keeping the temperature below 20° C. Upon completion, stirring is continued for 1 hour at room temperature and for one additional hour at 30°-35° C. The reaction mixture is evaporated in vacuo. The residue is taken up in toluene and the latter is evaporated again. The residue is distilled, yielding α-chloro-α-methyl-m-tolyl 2-thienyl ketone; b.p. 168°-178° C at 0.7 mm pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064132 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-88342299712d4d86b8a5501071183149 |
| Source note | uspto-grants-1977_12 |