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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051177Generated: October 31, 2026

Potassium Carbonate → HCID 131716893, compound

https://huagongshe.com/reaction/2051177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-(morpholin-4-yl)ethan-1-oneHCID 13996876—
ReactantHCID 67947591HCID 67947591—
ReactantHCID 67947630HCID 67947630—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 131716893HCID 13171689318%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-(2-Bromoacetyl)morpholine (7.3 g) in 2 butanone (50 cc) is added to a stirred suspension of a mixture (11.2 g of 5-fluoro-2-(4-methylphenyl)-4-quinolone and 7-fluoro-2-(4-methylphenyl)-4-quinolone and anhydrous potassium carbonate (11.3 g) in 2-butanone (250 cc). The mixture is heated to reflux for 15 hours and cooled to room temperature (approximately 20° C.), the insoluble matter is removed by filtration and the 2-butanone is evaporated off under reduced pressure. The residue is taken up with water (200 cc) and the aqueous phase is extracted with methylene chloride (3×100 cc). The organic phase is separated after settling has taken place, dried and evaporated under reduced pressure. After chromatography of the residue on silica gel by means of cyclohexane/ethyl acetate mixture (70:30 by volume) as eluant, the solid obtained is ground in 40°-60° C. petroleum ether (100 cc). 4-≡[5-fluoro-2-(4-methylphenyl-4-quinolyl]oxyacetyl}morpholine (2.4 g), m.p. 142°-4° C., is thereby obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017576
Source datasetuspto-grants-1991_05
ORD IDord-3f6e8878ee6c4ff297841baabf305469
Source noteuspto-grants-1991_05