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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410237Generated: October 31, 2026

Ethanol → 4-(2-Fluoropyridin-3-yl)cyclohexanol

https://huagongshe.com/reaction/410237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-(2-Fluoropyridin-3-YL)cyclohex-3-enolHCID 59326794—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Fluoropyridin-3-yl)cyclohexanolHCID 58547709—

Reaction Steps

To a flask containing 4-(2-fluoropyridin-3-yl)cyclohex-3-enol (750 mg, 3.88 mmol) and Ethanol (31.100 ml):Tetrahydrofuran (7.78 ml) was added 10% palladium on carbon, (240 mg, 2.255 mmol) before purging the reaction of air and backfilling with hydrogen. It was stirred for 3 h at room temperature before adding an additional 30 mol % Pd/C and stirring at 40° C. for 16 h. The reaction mixture was cooled and filtered through Celite before concentrating under reduced pressure to yield 4-(2-fluoropyridin-3-yl)cyclohexanol as a pale yellow oil that was used without purification. MS (ESI, pos. ion) m/z: 196.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-11fcbd2b58ca41f4a25218635d5488b1
Source noteuspto-grants-2014_06