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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075672Generated: October 31, 2026

Acetone → HCID 10491789, compound

https://huagongshe.com/reaction/1075672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl BromideHCID 7498—
Reactant8-Hydroxyquinoline-5-carbaldehydeHCID 275363—
ProductHCID 10491789HCID 1049178955.1%

Reaction Steps

To a solution of 8-hydroxyquinoline-5-carbaldehyde (346 mg, 2 mmol) in acetone (15 ml) anhydrous potassium carbonate (300 mg, 2.2 mmol) and benzylbromide (0.25 ml, 360 mg, 2.1 mmol) were added at 50° C. and the stirring was-continued for other 4 h at this temperature. The solvent was removed under reduced pressure, the residue taken up with dichloromethane, the organic layer washed several times with water, dried (sodium sulfate) and evaporated under vacuum. The residue was chromatographed on silica gel using as eluant ethylacetate/cyclohexane (2:3) to give 290 mg (55% yield) of 8-benzyloxyquinoline-5-carbaldehyde. The above obtained compound (290 mg, 1.1 mmol) was dissolved in ethanol (10 ml), then 2-oxindole (170 mg, 1.28 mmol) and piperidine (0.15 ml) were added and the, mixture maintained for 4 h at about 60° C. After cooling the precipitate was filtered, washed with cold ethanol and dried to give 300 mg (72% yield) of raw 3-(8-benzyloxyquinol-5-ylmethylen)-2-oxindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05905149
Source datasetuspto-grants-1999_05
ORD IDord-8fe3c570fffc4900aa69acab72edca1a
Source noteuspto-grants-1999_05