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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036277Generated: October 26, 2026

(+-)-2-Butanol → Tert-butyl 2-(2',3-difluoro-2,4'-bipyridin-5-yl)acetate

https://huagongshe.com/reaction/1036277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-2-ButanolHCID 6568—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoropyridine-4-boronic acidHCID 2783396—
ReactantTert-butyl 2-(6-chloro-5-fluoropyridin-3-yl)acetateHCID 58365072—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(2',3-difluoro-2,4'-bipyridin-5-yl)acetateHCID 58447733—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a flask containing tert-butyl 2-(6-chloro-5-fluoropyridin-3-yl)acetate 205-3 (370 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 20% ethyl acetate in dichloromethane to give tert-butyl 2-(2′,3-difluoro-2,4′-bipyridin-5-yl)acetate 205-5 as a yellow oil. MS m/z 307.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546396B2
Source datasetuspto-grants-2013_10
ORD IDord-7a3892ef55684abb9ec068f94c056739
Source noteuspto-grants-2013_10