HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482414Generated: October 31, 2026
Sulfuric Acid → 2-(4-Hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione
https://huagongshe.com/reaction/482414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(4-Isopropoxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione | HCID 18981072 | — |
| Product | 2-(4-Hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione | HCID 18981067 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05798316 |
|---|
| Source dataset | uspto-grants-1998_08 |
|---|
| ORD ID | ord-81dc6b7016e24da593f7006ac30f7449 |
|---|
| Source note | uspto-grants-1998_08 |
|---|