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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497321Generated: October 28, 2026

Thionyl Chloride → HCID 22318640, compound

https://huagongshe.com/reaction/497321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22318674HCID 22318674—
SolventBenzeneHCID 241—
ProductHCID 22318640HCID 22318640—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 8.3 g of 1-ethoxycarbonyl-4-[2-(4-fluorophenyl)-2-hydroxyethyl]piperazine hydrochloride were added 20 ml of benzene and 2.5 ml of thionyl chloride, followed by heating at 50° C. for 10 minutes. The reaction solution was concentrated under reduced pressure, 25% aqueous ammonia solution and water were poured, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and, after removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure. To the residue was poured 50 ml of 4M hydrogen chloride/ethyl acetate solution, the solution was concentrated under reduced pressure, and the resulting solid was washed with ether to give 8.1 g of 1-ethoxycarbonyl-4-[2-chloro-2-(4-fluorophenyl)ethyl]-piperazine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949552B2
Source datasetuspto-grants-2005_09
ORD IDord-d97d323f9731431fbd2170ae5c977cbe
Source noteuspto-grants-2005_09