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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504164Generated: October 25, 2026

Water → 6-(8-Bromooctyloxy)-2-methoxyquinoline

https://huagongshe.com/reaction/1504164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1,8-DibromooctaneHCID 78310—
Reactant6-Hydroxy-2-methoxyquinolineHCID 45091192—
SolventDimethylformamideHCID 6228—
Product6-(8-Bromooctyloxy)-2-methoxyquinolineHCID 66960886—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% in oil, 40 mg) was suspended in DMF(2 ml), and was cooled to 0° C. in ice water bath. 6-Hydroxy-2-methoxyquinoline(171 mg) was added thereto at the same temperature, and the mixture was stirred at 0° C. for an hour. 1,8-Dibromooctane(0.37 ml) was added thereto, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, followed by extraction using ethyl acetate. The organic layer was dried with sodium sulfate, and was condensed under reduced pressure. The residue was purified by silica gel column chromatography (hexane: ethyl acetate=10:1). The purified product was condensed to dryness under reduced pressure to give the title compound(225 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-09b94b0f72544cd19447b4e57e184c4d
Source noteuspto-grants-2015_12