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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292910Generated: October 27, 2026

Water → N-[4-(4-Pyridinylsulfonyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide

https://huagongshe.com/reaction/2292910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant4-SulfanilylpyridineHCID 459532—
Reactant3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2775125—
SolventDimethylacetamideHCID 31374—
ProductN-[4-(4-Pyridinylsulfonyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 986435360.4%

Reaction Steps

To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (4.28 g, 30.5 mmol) in N,N-dimethylacetamide (30 mL) was added thionyl chloride (3.63 g, 30.5 mmol) and the mixture stirred at -10° to -15° C. for one hour. 4-(4-Pyridylsulfonyl)benzenamine (4.77 g, 20.4 mmol) was added in one portion and the mixture stirred at room temperature overnight. The solution was poured into water, the yellow solid filtered and purified by flash chromatography (50% v/v ethyl acetate in methylene chloride). Evaporation of the eluent and trituration of the resulting solid with hot methylene chloride yielded the title propanamide (4.61 g, 60%) as an off-white solid; mp 255°-257° C. 1H-NMR (300 MHz, d6 -DMSO): 1.71 (s, 3H, CH3), 7.71 (s, 1H, OH), 8.01 (d, 2H, J=4.5 Hz, aromatic), 8.12 (d, 2H, J=7.1 Hz, aromatic), 8.19 (d, 2H, J=7.1 Hz, aromatic), 9.00 (d, 2H, J=4.5 Hz, aromatic), 10.61 (s, 1H, NH). MS (CI, CH4): 375(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684198
Source datasetuspto-grants-1997_11
ORD IDord-c32ca8da8dfc4d29b9b3f99081ce72f9
Source noteuspto-grants-1997_11