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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292961Generated: November 1, 2026

Thionyl Chloride → N-[4-(2-Pyridylcarbonyl)phenyl]-3,3-difluoro-2-hydroxy-2-difluoromethyl propionamide

https://huagongshe.com/reaction/2292961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Aminophenyl)-2-pyridinylmethanoneHCID 10726619—
Reactant2,2-Bis-difluoromethyl-2-hydroxyacetic acidHCID 22287454—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductN-[4-(2-Pyridylcarbonyl)phenyl]-3,3-difluoro-2-hydroxy-2-difluoromethyl propionamideHCID 2148010139.3%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 2,2-bis-difluoromethyl-2-hydroxyacetic acid (0.5 g, 2.84 mmoles) in dimethylacetamide (10 mL) at -10° C. was added thionyl chloride (0.34 g, 2.84 mmoles) dropwise. The resulting solution was stirred at -10° C. for approximately 30 mins. 4-(2-Pyridylcarbonyl)aniline (0.58 g, 2.5 mmoles) was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was then poured into water, sodium bicarbonate solution added to give a pH of 7 and extracted with ethyl acetate. The ethyl acetate extracts were combined, washed with water, brine, dried (Na2 SO4), decolorized (charcoal), and evaporated. The crude solid was dissolved in ether, clarified by filtration, and evaporated to give a yellow orange gum. Crystallization from methylene chloride/hexane gave the title compound (0.35 g, 35%) as a tan solid; mp 158°-161° C. 1H-NMR (300 MHz, d6 -DMSO); 6.48(t, J=54.12 Hz, 2H, HCF2), 7.67(t, J=6.18 Hz, 1H, ArH), 7.91-8.10 (m, 7H, ArH, OH), 8.73 (d, J=7.35 Hz, 1H, ArH), 10.40 (s, 1H, NH). MS(CI),CH4 : 357(M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684198
Source datasetuspto-grants-1997_11
ORD IDord-04d9710a2da447bb9559550cea234991
Source noteuspto-grants-1997_11