Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222285Generated: October 29, 2026

Water → 2-(6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide

https://huagongshe.com/reaction/2222285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-HydroxyquinolineHCID 11374—
ReactantSodium hydrideHCID 24758—
Reactant2-bromo-N-(4-methylpent-2-yn-4-yl)butyramideHCID 21078406—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-(6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramideHCID 69253949—

Reaction Steps

6-Hydroxyquinoline (0.46 g) in dry N,N-dimethylformamide (10 ml) was added dropwise to a stirred suspension of sodium hydride (0.10 g, 80% dispersion in mineral oil) in dry N,N-dimethylformamide under an atmosphere of nitrogen at ambient temperature. The green solution was stirred at ambient temperature for 1 hour and a solution of 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide (0.74 g) in dry N,N-dimethylformamide (10 ml) was added. The mixture was stirred at ambient temperature for 18 hours, poured into water and extracted into diethyl ether (three times). The organic extracts were combined, washed with dilute aqueous sodium hydroxide, water (twice), dried over magnesium sulphate and evaporated under reduced pressure to give a gum. The gum was fractionated by chromatography (silica; diethyl ether) to give the required product, 0.44 g, as a colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371764B2
Source datasetuspto-grants-2008_05
ORD IDord-e527ddbdcf464a129874042d2677f89f
Source noteuspto-grants-2008_05