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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257382Generated: October 31, 2026

Sulfuric Acid → 2-(4-Hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione

https://huagongshe.com/reaction/257382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-(4-Isopropoxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dioneHCID 18981072—
Product2-(4-Hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dioneHCID 18981067—

Reaction Conditions

Temperature0 °C

Reaction Steps

Concentrated sulfuric acid (5 mL) that had been cooled to 0°-5° C. was mixed with 2.80 g (0.010 mole) of 2-(4-isopropoxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione that had been cooled to 0° C. The mixture was maintained at 0° C. for ten minutes, during which time it became homogeneous. The mixture was then poured into ice-water, and the resulting mixture was extracted with ethyl acetate. The extract was washed in succession with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride. The extract was dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated from the filtrate under reduced pressure, leaving a residue. This residue was placed on a column of silica gel and eluted with ethyl acetate/hexane (1:1). After the product-containing fractions were combined and the solvents evaporated under reduced pressure, 1.38 g of 2-(4-hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione was recovered as a stiff syrup. The NMR was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262390
Source datasetuspto-grants-1993_11
ORD IDord-a42d3033ab5c41ac8ae49514147577c1
Source noteuspto-grants-1993_11