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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512284Generated: November 4, 2026

Ethanol → Ethyl 4-fluoro-3-hydroxybenzoate

https://huagongshe.com/reaction/1512284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Fluoro-3-hydroxybenzoic acidHCID 593635—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-fluoro-3-hydroxybenzoateHCID 1800771293%

Reaction Steps

To a solution of 4-fluoro-3-hydroxy-benzoic acid (2 g, 12.81 mmol) in absolute ethanol (30 ml) was added thionyl chloride (1 ml) drop wise at 0° C. After refluxing for overnight, the solvents were driven off, the residue was dissolved in dichloromethane (50 ml), cooled on ice bath, neutralized slowly with 1M NaHCO3, and the layers were separated. The aqueous layer was extracted with dichloromethane (50 ml) for one more time. Combined organic extracts were dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography using dichloromethane to yield 2.2 g (93%) of product. MS (ESI+) m/z 185 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217067B2
Source datasetuspto-grants-2012_07
ORD IDord-87f098d8a33f40d7afc7cf0428129b15
Source noteuspto-grants-2012_07