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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120360Generated: November 2, 2026

Potassium Iodide → (R)-N-[3-Iodo-2-chlorophenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide

https://huagongshe.com/reaction/2120360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetateHCID 8857—
ReactantSodium NitriteHCID 23668193—
Reactant(R)-N-[3-Amino-2-chlorophenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 58964770—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product(R)-N-[3-Iodo-2-chlorophenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 6953950677.6%

Reaction Steps

To a cooled solution of (R)-N-[3-amino-2-chlorophenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Method 32) (12.5 g) in concentrated sulphuric acid (25 ml) and water (70 ml) was added a solution of sodium nitrite (3.15 g) in water (70 ml) dropwise. The reaction mixture was allowed to stir for 10 minutes and for 1 hour at ambient temperature. A solution of potassium iodide (22.2 g) in water (70 ml) was added cautiously and the mixture was heated to 100° C. for 2.5 hours. The reaction mixture was allowed to cool to ambient temperature, EtOAc (500 ml) was added and the organic phase was washed with brine (300 ml) and dried. Volatile material was removed by evaporation and the residue was purified by flash column chromatography eluting with 5-20% EtOAc/isohexane to give the title compound (13.5 g) as a cream solid. NMR (CDCl3) 1.76 (s, 3H), 3.63 (s, 1H), 7.05 (t, 1H), 7.68 (d, 1H), 8.36 (d, 1H), 8.97 (brs, 1H); m/z: 392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689909B1
Source datasetuspto-grants-2004_02
ORD IDord-5b3d90078a244a7bb5da8cf099362c89
Source noteuspto-grants-2004_02