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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062370Generated: October 26, 2026

2-Fluorothiophenol → (R)-N-[2-Chloro-4-(2-fluorophenylsulphanyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide

https://huagongshe.com/reaction/1062370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorothiophenolHCID 520216—
ReactantSodium MethoxideHCID 10942334—
Reactant(R)-N-(2-chloro4-iodophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 54268602—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product(R)-N-[2-Chloro-4-(2-fluorophenylsulphanyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 54103294—

Reaction Steps

Tetrakis(triphenylphosphine)palladium(0) (0.147 g) was added to a deoxygenated mixture of (R)-N-(2-chloro-4-iodophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Example 197) (1.0 g), 2-fluorothiophenol (0.263 ml) and sodium methoxide (0.288 g) in ethanol (50 ml). The mixture was then further deoxygenated by evacuation and refilling with argon (3 cycles), and then heated under reflux with stirring under argon for 18 hours. The mixture was treated with a further portion of tetrakis(triphenylphosphine)palladium(0) (0.147 g), heated for a further 24 hours then cooled and filtered. Volatile material was removed by evaporation and the residue was purified by flash chromatography eluting with 20% ethyl acetate/hexane to give the title compound (0.906 g) as an oil. NMR (CDCl3): 1.75 (s, 3H), 3.58 (s, 1H), 7.1 (t, 2H), 7.2-7.35 (m, 3H), 7.37 (d, 1H), 8.3 (d, 1H), 8.82 (brs, 1H); MS (ESP−): 392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960688B2
Source datasetuspto-grants-2005_11
ORD IDord-f7a153da70b843139bab69fc2f6c24b8
Source noteuspto-grants-2005_11