Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384118Generated: October 30, 2026

Citric Acid → HCID 86641942, compound

https://huagongshe.com/reaction/384118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantHydrochloric AcidHCID 313—
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 46311240HCID 46311240—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventDiisobutylaluminumhydrideHCID 21225700—
ProductHCID 86641942HCID 86641942—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 6-chloro-3-fluoropyridin-2-carboxylic acid methyl ester (245 mg) in dimethylformamide (3 ml), 200 mg of phenol and 393 mg of potassium carbonate were added, and the reaction solution was stirred at 100° C. for 1.5 hours. The reaction solution was cooled, then 1N hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to afford a crude product as a brown oil. To a solution of the crude product in toluene (5 ml), 9.9 ml of diisobutylaluminum hydride (1.0M hexane solution) was added at −78° C., and the reaction solution was stirred for 2 hours while increasing the temperature of the reaction solution to room temperature. To the reaction solution were added water and 10% aqueous citric acid sequentially, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (98:2-50:50)) to afford the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367708B2
Source datasetuspto-grants-2013_02
ORD IDord-14d89ee2882e4809af2adf771bbc64fd
Source noteuspto-grants-2013_02