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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052889Generated: October 31, 2026

Chloride → 1-(4-Fluorophenyl)-5-(morpholin-4-yl)pentane-1,5-dione

https://huagongshe.com/reaction/1052889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Fluorobenzoyl)butyric AcidHCID 689096—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
Product1-(4-Fluorophenyl)-5-(morpholin-4-yl)pentane-1,5-dioneHCID 58070809—

Reaction Steps

10 gms of 5-(4-Fluoro-phenyl)-5-oxo-pentanoic acid and 5.6 gms of triethyl amine was added to 25 ml of toluene. 5.1 gms of Pivollyl chloride was added and stirred the reaction mass at room temperature for about 2 hours. 4 ml of Morpholine in 25 ml of toluene was added to the reaction mass at 0° C. Stirred the reaction mass for about 30 minutes at 0-5° C. and 20 ml of water was added. To the reaction mass 30 ml of brine solution was added and organic layer was separated. Dried the separated organic layer over sodium sulfate. Distill off the solvent completely under reduced pressure at 50-55° C. The resulted oily mass was dissolved in 12 ml of toluene and 60 ml of hexane. Cooled the reaction mass and 12 ml of toluene was added. Stirred the reaction mass for about 1-2 hours at 0-5° C., filtered, washed with 5 ml of hexane and dried at 40-45° C. to get 10 gms of 1-(4-Fluoro-phenyl)-5-morpholin-4-yl-pentane-1,5-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388440B2
Source datasetuspto-grants-2016_07
ORD IDord-bd6412aed8c1478bb104936a84bddeda
Source noteuspto-grants-2016_07