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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036286Generated: November 1, 2026

(+-)-2-Butanol → Ethyl 2-(2'-fluoro-2,4'-bipyridin-5-yl)acetate

https://huagongshe.com/reaction/1036286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-2-ButanolHCID 6568—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoropyridine-4-boronic acidHCID 2783396—
ReactantEthyl 2-(6-chloropyridin-3-yl)acetateHCID 15661146—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(2'-fluoro-2,4'-bipyridin-5-yl)acetateHCID 58447698—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a flask containing ethyl 2-(6-chloropyridin-3-yl)acetate 208-1 (300 mg, 1.5 mmol), 2-fluoropyridin-4-ylboronic acid 205-4 (318 mg, 2.25 mmol), Pd(OAc)2 (17 mg, 0.075 mmoL), 2-dicyclohexylphosphino-2′,6′-dimethoxyybiphenyl (62 mg, 0.15 mmol), K3PO4 (800 mg, 9 mmol) under argon was added 2-butanol (1.5 mL). The reaction mixture was stirred at 100° C. for 10 hours. After cooled to room temperature, the mixture was diluted with ethyl acetate, washed with water and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude was purified by silica gel flash chromatography, eluted with 40% ethyl acetate in dichloromethane to give ethyl 2-(2′-fluoro-2,4′-bipyridin-5-yl)acetate 208-2 as a yellow solid. MS m/z 261.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546396B2
Source datasetuspto-grants-2013_10
ORD IDord-b8cf8103d64648ecafda12dea2503dc3
Source noteuspto-grants-2013_10