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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192550Generated: November 1, 2026

Hydrochloric Acid → 1-(5-Chloro-8-hydroxy-7-quinolinyl)ethanone

https://huagongshe.com/reaction/1192550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Chloro-8-hydroxyquinolineHCID 2817—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium HydroxideHCID 14798—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(5-Chloro-8-hydroxy-7-quinolinyl)ethanoneHCID 1904345624.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5-chloro-8-quinolinol (6.67 g, 37.1 mmol, from Aldrich), aluminum trichloride (20.00 g, 150.0 mmol), and acetyl chloride (12.1 mL, 170 mmol) was stirred at 0° C. for 4 hours, then heated at 130° C. for 12 hours, cooled, and decomposed with water (39 mL) (caution!) and conc. HCl (13 mL). The solid product was filtered, and dried under reduced pressure. The solid obtained was then dissolved in 50 mL of water. To the solution was added 100 mL of dichloromethane. The mixture was cooled with an ice bath and its pH was adjusted to 4 with 20% NaOH. The mixture was filtered under reduced pressure. The solid collected was washed with water and air dried to give the desired product (˜2 g). The layers of the filtrate were separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with water, brine, dried over magnesium sulfate and concentrated to give additional desired product (total 5.6 g, 68%). LCMS calculated for C11H9ClNO2 (M+H)+: m/z=222.0; Found: 222.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-97c455dde0b94faf9031d00d9189945b
Source noteuspto-grants-2014_03