Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420582Generated: November 1, 2026

Thionyl Chloride → HCID 57966568, compound

https://huagongshe.com/reaction/420582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-[1-(6-Chlorobenzothiazole-2-yl)-4-ethyl piperidine-4-yl]ethanolHCID 57966704—
ProductHCID 57966568HCID 5796656892%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-[1-(6-chlorobenzothiazole-2-yl)-4-ethyl piperidine-4-yl]ethanol (764 mg) and thionyl chloride (4 mL) were stirred at 60° C. for 1.5 hours. To the reaction solution was added ice and extracted with ethyl acetate. The organic layer was washed with sodium hydrogencarbonate and brine and dried over sodium sulphate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatograph on silica gel to give the title compound (739 mg). Yield: 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097610B2
Source datasetuspto-grants-2012_01
ORD IDord-3a597c77aaf34956b6c42a84b3d5e76d
Source noteuspto-grants-2012_01