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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377969Generated: November 1, 2026

Thionyl Chloride → HCID 22915621, compound

https://huagongshe.com/reaction/1377969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-(6-Methylquinolin-2-yl)benzamideHCID 22915631—
ProductHCID 22915621HCID 2291562111%

Reaction Steps

2.5 ml (34.2 mmol) of thionyl chloride were added to 1.28 g (4.88 mmol) of 2-(6-methylquinolin-2-yl)benzamide obtained in Reference Example 7 and the mixture was stirred. After heating the mixture under reflux for 3 hours, thionyl chloride was distilled off. The residue was dissolved in 100 ml of chloroform and poured into iced water. The organic layer was separated, neutralized with 150 ml of a saturated sodium bicarbonate solution, washed with a saturated sodium chloride solution and dried over magnesium sulfate followed by filtration. The resulting filtrate was concentrated and the concentrate was subjected to silica gel chromatography using a mixed solvent of hexane and ethyl acetate (10/1) to obtain 150 mg of 2-(4-chloro-6-methylquinolin-2-yl)benzo-nitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665881
Source datasetuspto-grants-1997_09
ORD IDord-58dc230cc19f4c44b6a570b468de1ae5
Source noteuspto-grants-1997_09