Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374874Generated: October 30, 2026

Sodium Hydroxide → HCID 11596645, compound

https://huagongshe.com/reaction/374874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2775125—
Reactant2-Chloro-5-(phenylsulphonyl)anilineHCID 3020773—
SolventDimethylacetamideHCID 31374—
ProductHCID 11596645HCID 1159664533.9%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution containing 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (2.00 g) in N,N-dimethylacetamide (40 mL) cooled to -20° C. was added thionyl chloride (1.50 g) and the mixture was stirred for 1.0 hour. 6-chloro-3-phenylsulfonylaniline (2.42 g) was added in one portion and mixture was stirred for 48 hours at room temperature. The reaction mixture was poured into aqueous sodium hydroxide (1.0N, 250 mL) and extracted with ethyl acetate. The combined ethyl acetate extracts were washed (aqueous sodium hydroxide, brine) and evaporated. Chromatography, with hexane:ethyl acetate as the eluent (4:1 then 2:1) yielded the title compound as a white solid (1.25 g); mp: 79°-80° C.; NMR (250 MHz): 1.61 (s,3), 7.69 (m,3), 7.82 (m,2), 7.94 (d,1, J=9), 7.98 (m,2), 8.52 (s,1), 9.93 (s,1); MS: m/z=408(M+1). Analysis for C16H13ClF3NO4S: Calculated: C, 47.11; H, 3.19; N, 3.44; Found: C, 47.10; H, 3.28; N, 3.38.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482969
Source datasetuspto-grants-1996_01
ORD IDord-b42cdd1cf9e645d290d4cbec2c04f782
Source noteuspto-grants-1996_01