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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33999Generated: October 23, 2026

Ammonium Chloride → (3-Fluorophenyl)-(3-fluoropyridin-2-yl)-methanol

https://huagongshe.com/en/reaction/33999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-FluoropyridineHCID 67794—
Reactant3-FluorobenzaldehydeHCID 68009—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product(3-Fluorophenyl)-(3-fluoropyridin-2-yl)-methanolHCID 23070231—

Reaction Conditions

Temperature-20 °C

Reaction Steps

Under nitrogen atmosphere, a solution of 9.75 g of diazabicyclo[2.2.0]octane in 150 mL of dehydrated diethyl ether was cooled to −40° C., added with 56 mL of 1.56 M n-butyllithium in hexane, and stirred at −20° C. for 1 hour. The solution was cooled to-60° C., added dropwise with 6.9 mL of 3-fluoropyridine, stirred at −60° C. for 1 hour, and added with 9.2 mL of 3-fluorobenzaldehyde. After stirring for 1 hour, aqueous ammonium chloride and ethyl acetate were successively added, and the mixture was recovered to room temperature. The organic layer was extracted, washed with water, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the resulting crude product was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:4), to give 12.6 g of the title compound as colorless needle crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-301457584e034ef78be9b798feba0750
Source noteuspto-grants-2008_09