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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461718Generated: October 25, 2026

Thionyl Chloride → alpha-Chloro-p-tolyl 2-thienyl ketone

https://huagongshe.com/reaction/461718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactantalpha-Hydroxy-p-tolyl 2-thienyl ketoneHCID 21391792—
SolventBenzeneHCID 241—
Productalpha-Chloro-p-tolyl 2-thienyl ketoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064132
Source datasetuspto-grants-1977_12
ORD IDord-0a63a6d00ba049ebbac099dcd1dee036
Source noteuspto-grants-1977_12