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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120352Generated: October 30, 2026

Phenol → HCID 69883467, compound

https://huagongshe.com/reaction/2120352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(2R)-N-[2-Chloro-4-(ethanesulfonyl)-3-fluorophenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamideHCID 57348891—
SolventDimethylformamideHCID 6228—
ProductHCID 69883467HCID 6988346719.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

(R)-N-[2-Chloro-3-fluoro-4-(ethylsulphonyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Example 15; 0.308 g) was added to a stirred suspension of phenol (0.150 g) and anhydrous potassium carbonate (0.220 g) in anhydrous DMF (2 ml). The reaction mixture was heated to 150° C. under argon for 17 hours and allowed to cool to ambient temperature. EtOAc (50 ml) was added and the organic phase was washed with brine (4×50 ml), separated, dried and volatile material was removed by evaporation. The residue was purified on a 8 g silica Biotage cartridge eluting 40% EtOAc/isohexane to give the title compound (0.073 g) as a pale yellow foam. NMR (CDCl3): 1.18 (t, 3H), 1.69 (s, 3H), 3.23-3.30 (q, 2H), 3.48 (s, 1H), 6.78 (d, 2H), 7.02 (t, 1H), 7.24 (t, 2H), 7.97 (d, 1), 8.50 (d, 1H), 9.24 (brs, 1H); m/z: 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689909B1
Source datasetuspto-grants-2004_02
ORD IDord-1da91b876204447db06a3d07f77dc5c7
Source noteuspto-grants-2004_02