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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63253Generated: October 26, 2026

Ethyl bromodifluoroacetate → Ethyl 2-(5-(4-cyanophenoxy)pyridin-2-yl)-2,2-difluoroacetate

https://huagongshe.com/reaction/63253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactant4-((6-Bromopyridin-3-yl)oxy)benzonitrileHCID 45142267—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(5-(4-cyanophenoxy)pyridin-2-yl)-2,2-difluoroacetateHCID 9005222356.5%

Reaction Steps

A mixture of ethyl 2-bromo-2,2-difluoroacetate (22.13 mL, 109.05 mmol) and copper (13.85 g, 218.1 mmol) in dry dimethylsulfoxide (DMSO) (80 mL) was stirred at room temperature (rt) for 4 h. 4-((6-Bromopyridin-3-yl)oxy)benzonitrile (10 g, 36.35 mmol) was added and the mixture heated at 50° C. for 16 h. The reaction mixture was cooled to room temperature, diluted with 200 mL of ethyl acetate (EtOAc) and stirred for 10 min. The mixture was filtered through a plug of Celite® and the filtrate was washed with saturated NH4Cl solution to remove any remaining copper. The solution was dried (Na2SO4) and solvent was removed under reduced pressure to give the title compound as brown oil (6.5 g, 56.5%): IR (thin film) 2229, 1767 cm−1; 1H NMR (300 MHz, CDCl3) δ 8.44 (d, J=2.7 Hz, 1H), 7.78 (d, J=8.7 Hz, 1H), 7.73-7.64 (m, 2H), 7.49 (dd, J=8.6, 2.7 Hz, 1H), 7.16-7.07 (m, 2H), 4.39 (q, J=7.1 Hz, 2H), 1.35 (t, J=7.2 Hz, 3H); ESIMS m/z 319 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447073B2
Source datasetuspto-grants-2016_09
ORD IDord-02423e094bc241c49175ffd10b6637c0
Source noteuspto-grants-2016_09