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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352332Generated: November 1, 2026

Thionyl Chloride → HCID 15631610, compound

https://huagongshe.com/reaction/2352332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 15631609HCID 15631609—
ProductHCID 15631610HCID 15631610—

Reaction Steps

Dissolved in 20 ml of thionyl chloride was 1.76 g of 1-(2-furanylcarbonyl)-4-(2-hydroxyethyl)piperazine. The resulting mixture was stirred at room temperature for 7.5 hours. The thionyl chloride was distilled off under reduced pressure and the residue was poured into cold water. After alkalinization of the resulting aqueous solution with sodium carbonate, the solution was extracted with benzene and the benzene layer was washed with water. The benzene layer was dried over anhydrous magnesium sulfate and thereafter concentrated under reduced pressure to give 1.2 g of an oily substance. The reaction product was provided for the next step in its unpurified form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876345
Source datasetuspto-grants-1989_10
ORD IDord-d511aea011ef45e290ab3558bab1095f
Source noteuspto-grants-1989_10