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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327215Generated: October 30, 2026

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

https://huagongshe.com/reaction/327215

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 (Na2SO4), 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 numberUS05272163
Source datasetuspto-grants-1993_12
ORD IDord-31bfabcf52bc4650af4e8bc0352ade93
Source noteuspto-grants-1993_12