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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259662Generated: October 27, 2026

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

https://huagongshe.com/reaction/2259662

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). Analysis for C15H13F3N2O4S: Calculated: C, 48.12; H, 3.51; N, 7.48 Found: C, 48.02; H, 3.59; N, 7.42

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474999
Source datasetuspto-grants-1995_12
ORD IDord-be8b58de29464119b5ed33f1790ac7e6
Source noteuspto-grants-1995_12