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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936495Generated: November 2, 2026

Trifluoroacetic acid → HCID 22382033, compound

https://huagongshe.com/reaction/1936495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium CarbonateHCID 10340—
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 22382050HCID 22382050—
ProductHCID 22382033HCID 2238203345%

Reaction Conditions

Temperature77.5 °C

Reaction Steps

To a solution of 1,4-dimethyl-6-(trifluoromethyl)-1H-pyridin-2-one (1.44 g, 7.23 mmol), trifluoroacetic acid (9 mL) and trifluoroacetic anhydride (1.53 mL, 10.85 mmol) was added NIS (2.569 g, 10.85 mmol) at room temperature. Then, the mixture was heated to 70-85° C. and was stirred for 2 h. The reaction mixture was cooled to room temperature and saturated sodium carbonate solution was added slowly to neutralize the solution. Then, the aqueous mixture was extracted with ethyl acetate (2×50 mL). The combined extracts were washed successively with saturated sodium thiosulfate solution (100 mL) and brine solution (100 mL) and were dried over anhydrous sodium sulfate. Filtration of the drying agent and concentration of the solvent gave a crude product, which was purified by silica gel chromatography on a Biotage (40m) column to afford 1.02 g (45% yield) of 1,4-dimethyl-3-iodo-6-(trifluoromethyl)-1H-pyridin-2-one as an amorphous white solid. ES-LRMS: m/z 318.1 (M+H), 381.2 (M+Na+CH3CN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388084B1
Source datasetuspto-grants-2002_05
ORD IDord-4fb816a998c948c8967bbfa300ec911d
Source noteuspto-grants-2002_05