Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788732Generated: November 3, 2026

Thionyl Chloride → HCID 5007017, compound

https://huagongshe.com/reaction/1788732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantNanofinHCID 68843—
Reactant2-(2-chlorophenyl)quinoline-4-carboxylic acidHCID 269171—
ProductHCID 5007017HCID 5007017—

Reaction Steps

2-(2-Chlorophenyl)-quinoline-4-carboxylic acid (5.7 g) and thionyl chloride (15 ml) are heated under reflux for 1 hour. The thionyl chloride is evaporated off, the residue is taken up in toluene (40 ml) and the toluene is also evaporated off. Toluene (50 ml) is then added to the residue obtained, followed by the dropwise introduction of 2,6-dimethylpiperidine (6.78 g), with stirring. The mixture is stirred for 1 hour at ambient temperature, the precipitate is filtered off and the filtrate is evaporated under reduced pressure. The residue is taken up in water (50 ml) and chloroform (50 ml). The organic phase is decanted and the aqueous phase is extracted with chloroform (50 ml). The organic phases are combined, dried over magnesium sulphate and evaporated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684652
Source datasetuspto-grants-1987_08
ORD IDord-4819cb8d9f104efaad3295b34f3731f5
Source noteuspto-grants-1987_08