Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273733Generated: October 26, 2026

4-Cyanopyridine → 4-(2,5-Difluorobenzoyl)pyridine

https://huagongshe.com/reaction/273733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanopyridineHCID 7506—
ReactantTetrahydrofuranHCID 8028—
Reactant1,4-DifluorobenzeneHCID 10892—
ReactantPentamethyldiethylenetriamineHCID 18196—
ReactantButyllithiumHCID 178418339—
Product4-(2,5-Difluorobenzoyl)pyridineHCID 1899845251.5%

Reaction Conditions

Temperature-75 °C

Reaction Steps

Butyl lithium (70 ml of 2.22M solution, 155 mmole) was added to a solution of pentamethyldiethylenetriamine (23.3 ml, 155 mmole) in THF (250 ml) at -70° C. The solution was stirred for 5 min and 1,4-difluorobenzene (17.7 g, 155 mmole) in THF was added at -70° C. The solution was stirred for 2 hr during which time it was cooled to -75° C. and 4-cyanopyridine (15.6 g, 150 mmole) in THF was added at -75° C. The mixture was allowed to warm to 25° C. slowly and then quenched with ammonium chloride solution. The mixture was diluted with ether and the organic layer was separated. The organic layer was washed with water and 3N hydrochloric acid. The acid washes were stirred for 2 hr and basified with sodium hydroxide. The basic mixture was extracted with ether and the ether solution concentrated in vacuo. The crude product was purified by chromatography on silica eluting with ethyl acetate-hexane (20:1) to give 4-(2,5-difluorobenzoyl)pyridine (16.9 g, 51.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387593
Source datasetuspto-grants-1995_02
ORD IDord-d4313a586a554ae8967446c481bfa571
Source noteuspto-grants-1995_02