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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259693Generated: November 4, 2026

Water → N-[4-(2-Cyanophenylsulfonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide

https://huagongshe.com/reaction/2259693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2775125—
ReactantHCID 10753680HCID 10753680—
SolventDimethylacetamideHCID 31374—
ProductN-[4-(2-Cyanophenylsulfonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamideHCID 1069223472%

Reaction Steps

To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro2-hydroxy-2-methylpropanoic acid (0.82 g, 5.2 mmol) in N,N-dimethylacetamide (10 mL) was added thionyl chloride (0.62 g, 5.2 mmol) and the mixture stirred at -10° to -15° C. for 1 hour. 4-[(2-Cyanophenyl)sulfonyl]benzeneamine (1.00 g, 3.8 mmol) was added in one portion and the reaction mixture stirred at room temperature overnight. The mixture was poured into water and the aqueous solution decanted from an oily solid which was purified by flash column chromatography (5% v/v ethyl acetate/methylene chloride). Recrystallization from methylene chloride/hexane yielded the title propanamide as a white solid (1.08 g, 72%); mp 156°-158° C. 1H-NMR (250 MHz, d6-DMSO): 1.58 (s, 3H, CH3) 7.59 (s, 1H, OH) 7.88-8.13 (m, 7H, aromatic) 8.31 (d, 1H, J=6.9 Hz, aromatic) 10.50 (s, 1H, OH). MS (CI, CH4): 399 (M+1). Analysis for C17H13F3N2O4S.0.50 H2O: Calculated: C, 50.12; H, 3.46; N, 6.87. Found: C, 49.86; H, 3.17; N, 6.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474999
Source datasetuspto-grants-1995_12
ORD IDord-12f30d82ccdc4cb5806dfab8f4014da9
Source noteuspto-grants-1995_12