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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684572Generated: October 31, 2026

Benzoylacetone → HCID 19039879, compound

https://huagongshe.com/reaction/1684572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylacetoneHCID 7166—
Reactant2-Amino-3',4',4,5-tetramethoxybenzophenone hydrochlorideHCID 21466134—
SolventEthanolHCID 702—
ProductHCID 19039879HCID 1903987970%

Reaction Steps

A mixture of 2-amino-4,5,3',4'-tetramethoxy-benzophenone hydrochloride (2.0 g), benzoylacetone (0.917 g) and ethanol (35 ml) was stirred under reflux for 1 hour. The reaction mixture was concentrated under reduced pressure. The residue was poured into a saturated aqueous solution of sodium bicarbonate, and the mixture was extracted with chloroform. The chloroform layer was washed with water, dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with chloroform-ethyl acetate (10:1, v/v) gave 3-benzoyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-methylquinoline (1.75 g, 70%). This compound was recrystallized from ethanol to give colorless prisms, mp. 151°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641788
Source datasetuspto-grants-1997_06
ORD IDord-03f9dcf9fe014bb4a1bd18ba671202ca
Source noteuspto-grants-1997_06