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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741838Generated: October 31, 2026

Water → 4-(Furan-3-yl)-7-methylquinoline

https://huagongshe.com/reaction/741838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Chloro-4-(furan-3-yl)quinolineHCID 23370170—
ReactantHCID 178418689HCID 178418689—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
Product4-(Furan-3-yl)-7-methylquinolineHCID 23370177—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a mixture of 7-chloro-4-(furan-3-yl)quinoline (30.2 g) and [1,3-bis(diphenylphosphino)propane]nickel (II) chloride (7.1 g) in Et2O (950 mL) was added MeMgBr (141 mL, 1.4M in 3:1 THF:toluene) at such a rate to maintain a temperature of 30° C. The mixture was refluxed for 30 min., cooled to 0° C. and saturated NH4Cl (200 mL) was added followed by H2O (100 mL). The layers were separated and the aqueous phase was extracted with EtOAc. The combined organics were washed with NH4OAc buffer, brine, dried (MgSO4) and concentrated. Chromatography (silica gel;EtOAc/hexane (3:7)) provided the title compound as a beige oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552437
Source datasetuspto-grants-1996_09
ORD IDord-07cefc43d8834002ad853d126d18dce2
Source noteuspto-grants-1996_09