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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754342Generated: October 31, 2026

Pyridine → HCID 532222, compound

https://huagongshe.com/reaction/1754342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-BromoanilineHCID 7807—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
SolventDichloromethaneHCID 6344—
ProductHCID 532222HCID 53222266.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred and 0° C. cooled solution of 4-bromoaniline (1.0 g, 5.8 mmol, 1.0 eq) and pyridine (0.61 mL, 7 mmol, 1.2 eq) in DCM (20 mL) was added drop wise a solution of 2,6-difluorobenzoyl chloride (0.8 mL, 6.4 mmol, 1.1 eq) in DCM (5 mL). After stirring the resulting mixture at the same temperature for 1 h, the solvent was removed under vacuum. The residue was taken into ethyl acetate (20 mL) and water (20 mL). The layers were separated. The aqueous layer was extracted with ethyl acetate (2×20 mL) and the combined organic layers were washed with brine (20 mL), dried (Na2SO4) and filtered. The filtrate was concentrated under vacuum to afford 1.20 g of the desired product as a white solid. 1HNMR (400 MHz, DMSO-d6) δ 7.78 (brs, 1H, D2O exchangeable), 7.53-7.37 (m, 5H), 7.02-6.95 (m, 2H); ESI-MS (m/z) 312, 314 [(MH)+ Br79,81].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169242B2
Source datasetuspto-grants-2015_10
ORD IDord-14c679d63a7d40dca479023d88144b58
Source noteuspto-grants-2015_10